search
Back to results

The Dual Antiplatelet Therapy Study (DAPT Study)

Primary Purpose

Coronary Artery Disease

Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Placebo & Aspirin
Clopidogrel & Aspirin, Prasugrel & Aspirin
Sponsored by
Baim Institute for Clinical Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring Acute Coronary Syndrome, Adverse event, Antiplatelet therapy, Sirolimus, Everolimus, Paclitaxel, Zotarolimus, Bare Metal Stent, Drug Eluting Stent, Clinical Events Committee, Dual antiplatelet therapy, Harvard Clinical Research Institute, Major Adverse Cardiac and Cerebral Event, Major Bleeding, Myocardial infarction, Myocardial ischemia, Percutaneous coronary intervention, Stent placement, Stent Thrombosis, Thienopyridine, Clopidogrel, Prasugrel

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria (Enrollment):

  1. Subject is > 18 years of age.
  2. Subjects undergoing percutaneous intervention with stent deployment (or has w/in 24 hours).
  3. Subjects without known contraindication to dual antiplatelet therapy for at least 30 months after enrollment and stent implantation.
  4. The subject has consented to participate and has authorized the collection and release of his medical information by signing the "Patient Informed Consent Form". The informed consent will be valid for the duration of the trial or until the subject withdraws.

Inclusion Criterion (Randomization at 12 months):

1. Subject, at 12 months, is free from death, MI, stroke, repeat coronary revascularization, major bleeding, and stent thrombosis and has been compliant with dual antiplatelet therapy following stent implantation.

Exclusion Criteria (Enrollment):

  1. Index procedure stent placement with stent diameter <2.25 mm or >4.0 mm.
  2. Pregnant women.
  3. Planned surgery necessitating discontinuation of antiplatelet therapy within the 30 months following enrollment.
  4. Current medical condition with a life expectancy of less than 3 years.
  5. Concurrent enrollment in another device or drug study whose protocol specifically excludes concurrent enrollment or that involves blinded placement of a DES or BMS other than those included as DAPT Study devices. The subject may only be enrolled in the DAPT Study once.
  6. Subjects on warfarin or similar anticoagulant therapy.
  7. Subjects with hypersensitivity or allergies to one of the drugs or components indicated in the Instructions for Use for the device implanted.
  8. Subjects unable to give informed consent.
  9. Subject treated with both DES and BMS during the index procedure.

Exclusion Criteria (Randomization at 12 months):

  1. Pregnant women.
  2. Subject switched thienopyridine type or dose within 6 months prior to randomization.
  3. Percutaneous coronary intervention or cardiac surgery between 6 weeks post index procedure and randomization.
  4. Planned surgery necessitating discontinuation of antiplatelet therapy within the 21 months following randomization.
  5. Current medical condition with a life expectancy of less than 3 years.
  6. Subjects on warfarin or similar anticoagulant therapy.

Sites / Locations

  • Thomas Hospital
  • Mercy Gilbert Medical Center
  • Heart & Vascular Center of Arizona
  • Scottsdale Health Care
  • NEA Baptist Clinic
  • University of Arkansas (Central VA) for Medical Science
  • Arkansas Heart Hospital
  • California Cardiovascular Consultants/ Washington Hospital
  • The Foundation for Cardiovascular Medicine
  • Mercy General Hospital
  • UC San Diego Medical Center
  • California Pacific Medical Center
  • St. Joseph's Medical Center- CA
  • Torrance Memorial Medical Center / Vasek Polak Research Program
  • Harbor - UCLA Medical Center
  • Medical Center of Aurora
  • Connecticut Clinical Research, LLC
  • Bridgeport Hospital
  • St. Vincent's Medical Center
  • Washington Hospital Center
  • Palm Beach Heart Research Institute
  • Bay Area Cardiology Associates/ Brandon Regional Hospital
  • Jacksonville Heart Center
  • Watson Clinic Center for Research
  • Diagnostic Cardiology Associates
  • Melbourne Internal Medicine Assoc
  • Baptist Hospital of Miami
  • Munroe Regional Medical Center
  • Ocala Regional Medical Center
  • Florida Hospital
  • Baptist Hospital
  • Sacred Heart Hospital
  • Tallahassee Memorial Hospital
  • Pepin Heart Hospital
  • Winter Haven Hospital
  • Emory University Hospital Midtown
  • Piedmont Hospital Research Institute
  • Emory University Hospital
  • Medical Center Central Georgia
  • Redmond Regional Hospital
  • Advocate Good Shephard Hospital
  • Jesse Brown VA Medical Center
  • Rush University Medical Center
  • University of Illinois at Chicago
  • Good Samaritan Hospital- IL
  • Elmhurst Memorial Hospital
  • Heartland Education and Research Foundation
  • Loyola University Medical Center
  • Heart Care Research Foundation
  • Edward Heart Hospital
  • Midwest Cardiovascular Research and Education Foundation
  • St. Vincent Heart Center of Indiana, LLC
  • Northwest Indiana Cardiovascular Physicians, P.C.
  • McFarland Clinic PC
  • St. Luke's Hospital - Cedar Rapids
  • Iowa Heart Center
  • Kings Daughters Medical Center
  • Tulane University Medical School
  • Northeast Cardiology Associates
  • Maine Medical Center
  • Sinai Hospital at Baltimore
  • Union Memorial Hospital
  • Shah Associates, LLC
  • Peninsula Regional Medical Center
  • Washington Adventist Hospital
  • Brigham and Women's Hospital
  • Boston Medical Center
  • Brigham and Women's Hospital
  • Beth Israel Deaconess Medical Center
  • Lahey Clinic Medical Center
  • Cape Cod Hospital
  • UMass Memorial Medical Center
  • Bay Regional Medical Center
  • Harper University Hospital
  • Henry Ford Hospital Heart & Vascular Institute
  • Borgess Medical Center
  • St. Joseph Mercy-PTCMI
  • William Beaumont Hospital
  • Covenant Medical Center
  • Great Lakes Heart & Vascular Institute, PC
  • Munson Medical Center
  • Beaumont Hospital Troy
  • Mayo Clinic - Saint Marys Hospital
  • Central Minnesota Heart Center at St. Cloud Hospital
  • Hattiesburg Clinic
  • Cardiology Associates Research LLC
  • St. Luke's Hospital Mid America Heart Institute
  • Kansas City Heart Foundation
  • North Kansas City Hospital
  • Washington University Hospital
  • St. Louis University Hospital
  • St. John's Mercy Medical Center
  • St. John's Medical Institute
  • Nebraska Heart Institute
  • Alegent Health / Bergan Mercy Hospital
  • Creighton University
  • Catholic Medical Center
  • Cooper University Hospital
  • Cardiovascular Associates of the Delaware Valley, PA
  • Hamilton Cardiology Associates
  • Valley Hospital
  • UMDNJ - Robert Wood Johnson Medical School
  • St. Michaels Hospital
  • Presbyterian Heart Group
  • SJH Cardiology Associates
  • Winthrop University Hospital
  • Hudson Valley Heart Center
  • Stony Brook University Medical Center
  • St. Elizabeth's Medical Center- NY
  • Westchester Medical Center
  • Asheville Cardiology Associates
  • Carolinas Medical Center
  • Carolina Heart Specialists
  • Carolina Cardiology Associates
  • Wake Heart Association
  • Forsyth Medical Center
  • Wake Forest Health Sciences
  • MeritCare Medical Center
  • Altru Health System
  • The Lindner Clinical Trial Center
  • Good Samaritan Hospital
  • University of Cincinnati Medical Center
  • Riverside Methodist
  • Elyria Memorial Hospital
  • Frederick C Smith Clinic dba Smith Clinic
  • Northwest Ohio Cardiology
  • Midwest Regional Medical Center
  • University of Oklahoma Health Sciences Center
  • Oklahoma Foundation for CV Research
  • St. Vincent Hospital/ Providence Heart Hospital
  • Oregon Health & Sciences University Hospital
  • Abington Memorial Hospital
  • Chambersburg Hospital
  • Geisinger Clinic
  • Doylestown Hospital
  • Pinnacle Health Hospital
  • Conemaugh Memorial Medical Center
  • UPMC Presbyterian Hospital
  • Donald Guthrie Foundation for Education and Research
  • Berks Cardiologists
  • York Hospital (PA)
  • Rhode Island Hospital
  • Miriam Hospital
  • AnMed Health
  • Black Hills Research- Rapid City Regional
  • North Central Heart Institute
  • Sanford USD Medical Center
  • Chattanooga Heart - East Third Street
  • Chattanooga Heart Institute
  • Centennial Heart Medical Center
  • Austin Heart
  • Capital Cardiovascular Research Institute
  • Texas Cardiovascular
  • Veteran's Affairs Medical Center- Dallas
  • CRSTI Research
  • UT Southwestern Medical Center
  • Methodist DeBakey Heart & Vascular Center
  • North Dallas Research Associates
  • North Dallas Research Associate
  • The Heart Hospital / Baylor Plano
  • Scott and White Healthcare - Round Rock
  • TexSan Heart Hospital
  • Mother Frances Hospital
  • Providence Healthcare Network
  • Intermountain Medical Center
  • University of Virginia
  • Rockingham Memorial Hospital
  • Lynchburg General Hospital
  • Sentara, Norfolk General Hospital
  • Carilion Clinic
  • Cardiovascular Associates, Ltd.
  • Winchester Medical Center
  • Providence St. Peter Hospital
  • University of Washington
  • Inland Cardiology Associates
  • Sacred Heart Medical Center
  • Aurora St. Luke's Medical Center
  • CaRE Foundation, Inc.
  • St. Vincents Hospital Sydney
  • Prince of Wales Eastern Heart
  • Royal Adelaide Hospital
  • The Alfred Hospital
  • Fremantle Hospital
  • The Mount Hospital
  • Royal Perth Hospital
  • Monash Heart
  • St Vincents Hospital Melbourne
  • Fakultni nemocnice Hradec Kralove
  • Krajska karlovarska nemocnice a.s.
  • Centrum pro choroby srdce a cev
  • Mestska nemocnice Ostrava
  • Krajska nemocnice T. Bati a.s.
  • Centre Hospitalier Saint Louis
  • Hospital Saint Philibert
  • Nouvelles Cliniques Nantaises
  • Clinique les Franciscaines
  • Hopital Bichat
  • Groupe Hospitalier Sud
  • CH Chatiliez Tourcoing
  • Helios Klinikum Emil von Behring
  • Universitaetsklinikum Schleswig-Holstein - PS
  • Vivantes Klinikum im Friedrichshain
  • Vivantes-Klinikum Neukoelin
  • Vivantes-Klinikum Neukoelln
  • Vivantes-Humboldt Klinikum
  • Elbe-Kliniken Stade-Buxtehude GmbH
  • Universitaetsklinikum Dresden
  • Asklepios Klinik St. Georg
  • Herzzentrum Leipzig GmbH
  • Elbe-Kliniken Stade-Buxtehude GmbH
  • Gottsegen Gyorgy Orszagos Kardiologiai Intezet
  • Josa Andras Oktato Korhaz Nonprofit Kft
  • Pecsi Tudomanyegyetem Klinikai Kozpont
  • Szegedi Tudomanyegyetem Szent-Gyorgyi Klinikai Kozpont
  • Zala Megyei Korhaz
  • Mercy Angiography
  • North Shore Hospital
  • Ascot Hospital
  • Middlemore Hospital
  • Christchurch Hospital
  • Waikato Hospital
  • Nelson Hospital
  • Wellington Hospital
  • Wakefield Hospital
  • Uniwersyteck Szpital Klin. w Bialymstoku
  • Wielospecj. Szpital Miejski im.dr.E.Warminskiego-SPZOZ
  • NZOZ Centrum Medyczne Beluga-Med
  • Szpital Uniwersytecki w Krakowie
  • SPSK nr 2 Pomorskiej Akademii Medycznej w Szczecinie
  • Polsko-Amerykanskie Kliniki Serca.American Heart of Poland S
  • Instytut Kardiologii im. Kardynala St. Wyszynskiego
  • Centrul Clinic de Urgenta de Boli Cardiovasculare al Armatei
  • Spitalul Clinic de Urgenta Bucuresti
  • Inst. Urgenta Boli Cardiovasculare Prof. Dr. C.C. Iliescu
  • Institutul de Urgenta pentru Boli Cardiovasculare Prof. Dr.
  • Spitalul Clinic Universitar de Urgenta Bucuresti
  • Institutul Inimii Niculae Stancioiu Cluj-Napoca
  • Institutul de Boli Cardiovasculare si Transplant Targu Mures
  • Wycombe General Hospital
  • Papworth Hospital
  • Torbay hospital
  • Royal Bournemouth General Hospital
  • Basildon University Hospital
  • Barnet Hospital
  • James Cook Hospital
  • Ninewells Hospital
  • Weston General Hospital
  • Golden Jubilee National Hospital
  • St Peter's Hospital
  • University Hospital of Coventry and Warwickshire
  • Ninewells Hospital
  • Royal Infirmary of Edinburgh
  • University Hospital of Leicester Glenfield Hospital
  • The London Chest Hospital
  • Freeman Hospital
  • Derriford Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

12m DAPT Study Arm

30m DAPT Study Arm

Arm Description

This population consists of subjects enrolled in the study who are free from death, MI, stroke, repeat coronary revascularization, major bleeding, and ST 12 months after stent implantation and who are compliant with 12 months of dual antiplatelet therapy following stent implantation and who are subsequently randomized to receive 18 months of placebo treatment in addition to aspirin.

This population consists of subjects enrolled in the study who are free from death, MI, stroke, repeat coronary revascularization, major bleeding, and ST 12 months after stent implantation and who are compliant with 12 months of dual antiplatelet therapy following stent implantation and who are subsequently randomized to receive an additional 18 months of thienopyridine treatment in addition to aspirin.

Outcomes

Primary Outcome Measures

MACCE (Death, Myocardial Infarction or Stroke) - Randomized DES ITT
The coprimary efficacy endpoints were the cumulative incidence of MACCE and the cumulative incidence of ARC definite or probable stent thrombosis within randomized DES ITT patients between 12 and 30 months post procedure.
Definite or Probable Stent Thrombosis (ST) - Randomized DES ITT
The coprimary efficacy endpoints were the cumulative incidence of MACCE and the cumulative incidence of definite or probable ST within randomized DES ITT patients between 12 and 30 months post procedure. ST was assessed according to the Academic Research Consortium (ARC) definitions.
GUSTO Severe or Moderate Bleeding - Randomized DES ITT
The primary safety endpoint was moderate or severe bleeding within randomized DES ITT patients between 12 and 30 months post procedure. Bleeding was assessed according to the Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Arteries (GUSTO) criteria.

Secondary Outcome Measures

MACCE (Death, Myocardial Infarction or Stroke) - Propensity Matched DES vs. BMS
Secondary powered endpoint
Definite or Probable Stent Thrombosis (ST) - Propensity Matched DES vs. BMS
Secondary powered endpoint
MACCE (Death, Myocardial Infarction or Stroke) - Randomized DES ITT
Definite or Probable Stent Thrombosis (ST) - Randomized DES ITT
ST was assessed according to the Academic Research Consortium (ARC) definitions.
GUSTO Severe or Moderate Bleeding - Randomized DES ITT
Bleeding was assessed according to the Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Arteries (GUSTO) criteria.
MACCE (Death, Myocardial Infarction or Stroke) - Randomized BMS ITT
Definite or Probable Stent Thrombosis (ST) - Randomized BMS ITT
ST was assessed according to the Academic Research Consortium (ARC) definitions.
GUSTO Severe or Moderate Bleeding - Randomized BMS ITT
Bleeding was assessed according to the Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Arteries (GUSTO) criteria.
MACCE (Death, Myocardial Infarction or Stroke) - Randomized BMS ITT
Definite or Probable Stent Thrombosis (ST) - Randomized BMS ITT
ST was assessed according to the Academic Research Consortium (ARC) definitions.
GUSTO Severe or Moderate Bleeding - Randomized BMS ITT
Bleeding was assessed according to the Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Arteries (GUSTO) criteria.

Full Information

First Posted
September 14, 2009
Last Updated
May 10, 2017
Sponsor
Baim Institute for Clinical Research
Collaborators
Abbott, Boston Scientific Corporation, Bristol-Myers Squibb, Sanofi-Synthelabo, Cordis Corporation, Eli Lilly and Company, Daiichi Sankyo, Inc., Medtronic
search

1. Study Identification

Unique Protocol Identification Number
NCT00977938
Brief Title
The Dual Antiplatelet Therapy Study (DAPT Study)
Official Title
A Prospective, Multi-center, Randomized, Double-blind Trial to Assess the Effectiveness and Safety of 12 Versus 30 Months of Dual Antiplatelet Therapy in Subjects Undergoing Percutaneous Coronary Intervention With Either Drug-eluting Stent or Bare Metal Stent Placement for the Treatment of Coronary Artery Lesions
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
October 2009 (undefined)
Primary Completion Date
June 2014 (Actual)
Study Completion Date
June 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Baim Institute for Clinical Research
Collaborators
Abbott, Boston Scientific Corporation, Bristol-Myers Squibb, Sanofi-Synthelabo, Cordis Corporation, Eli Lilly and Company, Daiichi Sankyo, Inc., Medtronic

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The DAPT Study is a double blind randomized controlled trial intended to determine the appropriate duration for dual antiplatelet therapy (the combination of aspirin and a second anti-clotting medication) as well as the safety and effectiveness of dual antiplatelet therapy to protect patients from stent thrombosis and major adverse cardiovascular and cerebrovascular events (MACCE) following the implantation of drug-eluting coronary stents. Similar analysis will be conducted in a smaller cohort of bare metal coronary stent - treated subjects.
Detailed Description
Subjects with ischemic heart disease due to stenotic lesions in either native coronary arteries or coronary artery bypass grafts undergoing percutaneous coronary intervention (PCI) with stent placement and no contraindications to prolonged dual antiplatelet therapy are eligible to be enrolled in the study. All enrolled subjects will undergo PCI with stent placement. All enrolled subjects will be treated with either an FDA-approved drug eluting stent(s) (DES) or an FDA-approved bare metal stent(s) (BMS) (per their respective Instructions for Use) and assigned to 12 months of open label FDA-approved thienopyridine treatment in addition to aspirin. Operators will select the thienopyridine according to the package insert. Thienopyridine treatment dose will be according to the standard of practice and prescribing information for the selected medication. Aspirin treatment will be 75-325 mg for the first 6 months after the procedure and 75-162 mg subsequently, to be continued indefinitely. All DES or BMS subjects who are treated with 12 months of dual antiplatelet therapy post index procedure and who are event free per protocol will be eligible for randomization to either placebo (12 m DAPT Study arm) or an additional 18 months of thienopyridine treatment (30 m DAPT Study arm). Both arms will continue aspirin therapy. Up to four (4) separate post-market approval studies will be allowed to incorporate the randomized design of the DAPT Study for a subset of subjects who may then be contributed for the DAPT Study analyses.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease
Keywords
Acute Coronary Syndrome, Adverse event, Antiplatelet therapy, Sirolimus, Everolimus, Paclitaxel, Zotarolimus, Bare Metal Stent, Drug Eluting Stent, Clinical Events Committee, Dual antiplatelet therapy, Harvard Clinical Research Institute, Major Adverse Cardiac and Cerebral Event, Major Bleeding, Myocardial infarction, Myocardial ischemia, Percutaneous coronary intervention, Stent placement, Stent Thrombosis, Thienopyridine, Clopidogrel, Prasugrel

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
25682 (Actual)

8. Arms, Groups, and Interventions

Arm Title
12m DAPT Study Arm
Arm Type
Placebo Comparator
Arm Description
This population consists of subjects enrolled in the study who are free from death, MI, stroke, repeat coronary revascularization, major bleeding, and ST 12 months after stent implantation and who are compliant with 12 months of dual antiplatelet therapy following stent implantation and who are subsequently randomized to receive 18 months of placebo treatment in addition to aspirin.
Arm Title
30m DAPT Study Arm
Arm Type
Active Comparator
Arm Description
This population consists of subjects enrolled in the study who are free from death, MI, stroke, repeat coronary revascularization, major bleeding, and ST 12 months after stent implantation and who are compliant with 12 months of dual antiplatelet therapy following stent implantation and who are subsequently randomized to receive an additional 18 months of thienopyridine treatment in addition to aspirin.
Intervention Type
Drug
Intervention Name(s)
Placebo & Aspirin
Intervention Type
Drug
Intervention Name(s)
Clopidogrel & Aspirin, Prasugrel & Aspirin
Primary Outcome Measure Information:
Title
MACCE (Death, Myocardial Infarction or Stroke) - Randomized DES ITT
Description
The coprimary efficacy endpoints were the cumulative incidence of MACCE and the cumulative incidence of ARC definite or probable stent thrombosis within randomized DES ITT patients between 12 and 30 months post procedure.
Time Frame
18 months (12-30 months post-index procedure)
Title
Definite or Probable Stent Thrombosis (ST) - Randomized DES ITT
Description
The coprimary efficacy endpoints were the cumulative incidence of MACCE and the cumulative incidence of definite or probable ST within randomized DES ITT patients between 12 and 30 months post procedure. ST was assessed according to the Academic Research Consortium (ARC) definitions.
Time Frame
18 months (12-30 months post-index procedure)
Title
GUSTO Severe or Moderate Bleeding - Randomized DES ITT
Description
The primary safety endpoint was moderate or severe bleeding within randomized DES ITT patients between 12 and 30 months post procedure. Bleeding was assessed according to the Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Arteries (GUSTO) criteria.
Time Frame
18 months (12-30 months post-index procedure)
Secondary Outcome Measure Information:
Title
MACCE (Death, Myocardial Infarction or Stroke) - Propensity Matched DES vs. BMS
Description
Secondary powered endpoint
Time Frame
33 months (0-33 months post-index procedure)
Title
Definite or Probable Stent Thrombosis (ST) - Propensity Matched DES vs. BMS
Description
Secondary powered endpoint
Time Frame
33 months (0-33 months post-index procedure)
Title
MACCE (Death, Myocardial Infarction or Stroke) - Randomized DES ITT
Time Frame
21 months (12-33 months post-index procedure)
Title
Definite or Probable Stent Thrombosis (ST) - Randomized DES ITT
Description
ST was assessed according to the Academic Research Consortium (ARC) definitions.
Time Frame
21 months (12-33 months post-index procedure)
Title
GUSTO Severe or Moderate Bleeding - Randomized DES ITT
Description
Bleeding was assessed according to the Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Arteries (GUSTO) criteria.
Time Frame
21 months (12-33 months post-index procedure)
Title
MACCE (Death, Myocardial Infarction or Stroke) - Randomized BMS ITT
Time Frame
18 months (12-30 months post-index procedure)
Title
Definite or Probable Stent Thrombosis (ST) - Randomized BMS ITT
Description
ST was assessed according to the Academic Research Consortium (ARC) definitions.
Time Frame
18 months (12-30 months post-index procedure)
Title
GUSTO Severe or Moderate Bleeding - Randomized BMS ITT
Description
Bleeding was assessed according to the Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Arteries (GUSTO) criteria.
Time Frame
18 months (12-30 months post-index procedure)
Title
MACCE (Death, Myocardial Infarction or Stroke) - Randomized BMS ITT
Time Frame
21 months (12-33 months post-index procedure)
Title
Definite or Probable Stent Thrombosis (ST) - Randomized BMS ITT
Description
ST was assessed according to the Academic Research Consortium (ARC) definitions.
Time Frame
21 months (12-33 months post-index procedure)
Title
GUSTO Severe or Moderate Bleeding - Randomized BMS ITT
Description
Bleeding was assessed according to the Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Arteries (GUSTO) criteria.
Time Frame
21 months (12-33 months post-index procedure)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria (Enrollment): Subject is > 18 years of age. Subjects undergoing percutaneous intervention with stent deployment (or has w/in 24 hours). Subjects without known contraindication to dual antiplatelet therapy for at least 30 months after enrollment and stent implantation. The subject has consented to participate and has authorized the collection and release of his medical information by signing the "Patient Informed Consent Form". The informed consent will be valid for the duration of the trial or until the subject withdraws. Inclusion Criterion (Randomization at 12 months): 1. Subject, at 12 months, is free from death, MI, stroke, repeat coronary revascularization, major bleeding, and stent thrombosis and has been compliant with dual antiplatelet therapy following stent implantation. Exclusion Criteria (Enrollment): Index procedure stent placement with stent diameter <2.25 mm or >4.0 mm. Pregnant women. Planned surgery necessitating discontinuation of antiplatelet therapy within the 30 months following enrollment. Current medical condition with a life expectancy of less than 3 years. Concurrent enrollment in another device or drug study whose protocol specifically excludes concurrent enrollment or that involves blinded placement of a DES or BMS other than those included as DAPT Study devices. The subject may only be enrolled in the DAPT Study once. Subjects on warfarin or similar anticoagulant therapy. Subjects with hypersensitivity or allergies to one of the drugs or components indicated in the Instructions for Use for the device implanted. Subjects unable to give informed consent. Subject treated with both DES and BMS during the index procedure. Exclusion Criteria (Randomization at 12 months): Pregnant women. Subject switched thienopyridine type or dose within 6 months prior to randomization. Percutaneous coronary intervention or cardiac surgery between 6 weeks post index procedure and randomization. Planned surgery necessitating discontinuation of antiplatelet therapy within the 21 months following randomization. Current medical condition with a life expectancy of less than 3 years. Subjects on warfarin or similar anticoagulant therapy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Laura Mauri, MD, MSc
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Dean Kereiakes, MD, FACC
Organizational Affiliation
Christ Hospital Heart and Vascular Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Thomas Hospital
City
Fairhope
State/Province
Alabama
ZIP/Postal Code
36532
Country
United States
Facility Name
Mercy Gilbert Medical Center
City
Gilbert
State/Province
Arizona
ZIP/Postal Code
85297
Country
United States
Facility Name
Heart & Vascular Center of Arizona
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85006
Country
United States
Facility Name
Scottsdale Health Care
City
Scottsdale
State/Province
Arizona
ZIP/Postal Code
85258
Country
United States
Facility Name
NEA Baptist Clinic
City
Jonesboro
State/Province
Arkansas
ZIP/Postal Code
72401
Country
United States
Facility Name
University of Arkansas (Central VA) for Medical Science
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72205
Country
United States
Facility Name
Arkansas Heart Hospital
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72211
Country
United States
Facility Name
California Cardiovascular Consultants/ Washington Hospital
City
Fremont
State/Province
California
ZIP/Postal Code
94538
Country
United States
Facility Name
The Foundation for Cardiovascular Medicine
City
La Jolla
State/Province
California
ZIP/Postal Code
92037
Country
United States
Facility Name
Mercy General Hospital
City
Sacramento
State/Province
California
ZIP/Postal Code
95819
Country
United States
Facility Name
UC San Diego Medical Center
City
San Diego
State/Province
California
ZIP/Postal Code
92103-8784
Country
United States
Facility Name
California Pacific Medical Center
City
San Francisco
State/Province
California
ZIP/Postal Code
94115
Country
United States
Facility Name
St. Joseph's Medical Center- CA
City
Stockton
State/Province
California
ZIP/Postal Code
95204-6088
Country
United States
Facility Name
Torrance Memorial Medical Center / Vasek Polak Research Program
City
Torrance
State/Province
California
ZIP/Postal Code
90505
Country
United States
Facility Name
Harbor - UCLA Medical Center
City
Torrance
State/Province
California
ZIP/Postal Code
90509
Country
United States
Facility Name
Medical Center of Aurora
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80012
Country
United States
Facility Name
Connecticut Clinical Research, LLC
City
Bridgeport
State/Province
Connecticut
ZIP/Postal Code
06606
Country
United States
Facility Name
Bridgeport Hospital
City
Bridgeport
State/Province
Connecticut
ZIP/Postal Code
06610
Country
United States
Facility Name
St. Vincent's Medical Center
City
Stamford
State/Province
Connecticut
ZIP/Postal Code
06905
Country
United States
Facility Name
Washington Hospital Center
City
Washington, D.C.
State/Province
District of Columbia
ZIP/Postal Code
20010
Country
United States
Facility Name
Palm Beach Heart Research Institute
City
Atlantis
State/Province
Florida
ZIP/Postal Code
33462
Country
United States
Facility Name
Bay Area Cardiology Associates/ Brandon Regional Hospital
City
Brandon
State/Province
Florida
ZIP/Postal Code
33511
Country
United States
Facility Name
Jacksonville Heart Center
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207
Country
United States
Facility Name
Watson Clinic Center for Research
City
Lakeland
State/Province
Florida
ZIP/Postal Code
33805
Country
United States
Facility Name
Diagnostic Cardiology Associates
City
Lauderdale Lakes
State/Province
Florida
ZIP/Postal Code
33313
Country
United States
Facility Name
Melbourne Internal Medicine Assoc
City
Melbourne
State/Province
Florida
ZIP/Postal Code
32901
Country
United States
Facility Name
Baptist Hospital of Miami
City
Miami
State/Province
Florida
ZIP/Postal Code
33176
Country
United States
Facility Name
Munroe Regional Medical Center
City
Ocala
State/Province
Florida
ZIP/Postal Code
34471
Country
United States
Facility Name
Ocala Regional Medical Center
City
Ocala
State/Province
Florida
ZIP/Postal Code
34480
Country
United States
Facility Name
Florida Hospital
City
Orlando
State/Province
Florida
ZIP/Postal Code
32803
Country
United States
Facility Name
Baptist Hospital
City
Pensacola
State/Province
Florida
ZIP/Postal Code
32501
Country
United States
Facility Name
Sacred Heart Hospital
City
Pensacola
State/Province
Florida
ZIP/Postal Code
32504
Country
United States
Facility Name
Tallahassee Memorial Hospital
City
Tallahassee
State/Province
Florida
ZIP/Postal Code
32308
Country
United States
Facility Name
Pepin Heart Hospital
City
Tampa
State/Province
Florida
ZIP/Postal Code
33613
Country
United States
Facility Name
Winter Haven Hospital
City
Winter Haven
State/Province
Florida
ZIP/Postal Code
33881
Country
United States
Facility Name
Emory University Hospital Midtown
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30308
Country
United States
Facility Name
Piedmont Hospital Research Institute
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30309
Country
United States
Facility Name
Emory University Hospital
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Facility Name
Medical Center Central Georgia
City
Macon
State/Province
Georgia
ZIP/Postal Code
31201
Country
United States
Facility Name
Redmond Regional Hospital
City
Rome
State/Province
Georgia
ZIP/Postal Code
30165
Country
United States
Facility Name
Advocate Good Shephard Hospital
City
Barrington
State/Province
Illinois
ZIP/Postal Code
60010
Country
United States
Facility Name
Jesse Brown VA Medical Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Facility Name
Rush University Medical Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Facility Name
University of Illinois at Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Facility Name
Good Samaritan Hospital- IL
City
Downers Grove
State/Province
Illinois
ZIP/Postal Code
60515
Country
United States
Facility Name
Elmhurst Memorial Hospital
City
Elmhurst
State/Province
Illinois
ZIP/Postal Code
60126
Country
United States
Facility Name
Heartland Education and Research Foundation
City
Joliet
State/Province
Illinois
ZIP/Postal Code
60435
Country
United States
Facility Name
Loyola University Medical Center
City
Maywood
State/Province
Illinois
ZIP/Postal Code
60153
Country
United States
Facility Name
Heart Care Research Foundation
City
Mokena
State/Province
Illinois
ZIP/Postal Code
60448
Country
United States
Facility Name
Edward Heart Hospital
City
Naperville
State/Province
Illinois
ZIP/Postal Code
60540
Country
United States
Facility Name
Midwest Cardiovascular Research and Education Foundation
City
Elkhart
State/Province
Indiana
ZIP/Postal Code
46541
Country
United States
Facility Name
St. Vincent Heart Center of Indiana, LLC
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46290
Country
United States
Facility Name
Northwest Indiana Cardiovascular Physicians, P.C.
City
Valparaiso
State/Province
Indiana
ZIP/Postal Code
46383
Country
United States
Facility Name
McFarland Clinic PC
City
Ames
State/Province
Iowa
ZIP/Postal Code
50010
Country
United States
Facility Name
St. Luke's Hospital - Cedar Rapids
City
Cedar Rapids
State/Province
Iowa
ZIP/Postal Code
52403
Country
United States
Facility Name
Iowa Heart Center
City
West Des Moines
State/Province
Iowa
ZIP/Postal Code
50266
Country
United States
Facility Name
Kings Daughters Medical Center
City
Ashland
State/Province
Kentucky
ZIP/Postal Code
41101
Country
United States
Facility Name
Tulane University Medical School
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70112
Country
United States
Facility Name
Northeast Cardiology Associates
City
Bangor
State/Province
Maine
ZIP/Postal Code
04401
Country
United States
Facility Name
Maine Medical Center
City
Portland
State/Province
Maine
ZIP/Postal Code
04102
Country
United States
Facility Name
Sinai Hospital at Baltimore
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21215
Country
United States
Facility Name
Union Memorial Hospital
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21218
Country
United States
Facility Name
Shah Associates, LLC
City
Prince Frederick
State/Province
Maryland
ZIP/Postal Code
20678
Country
United States
Facility Name
Peninsula Regional Medical Center
City
Salisbury
State/Province
Maryland
ZIP/Postal Code
21804
Country
United States
Facility Name
Washington Adventist Hospital
City
Takoma Park
State/Province
Maryland
ZIP/Postal Code
20912
Country
United States
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
Boston Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02118
Country
United States
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02120
Country
United States
Facility Name
Beth Israel Deaconess Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States
Facility Name
Lahey Clinic Medical Center
City
Burlington
State/Province
Massachusetts
ZIP/Postal Code
01805
Country
United States
Facility Name
Cape Cod Hospital
City
Hyannis
State/Province
Massachusetts
ZIP/Postal Code
02601
Country
United States
Facility Name
UMass Memorial Medical Center
City
Worcester
State/Province
Massachusetts
ZIP/Postal Code
01655
Country
United States
Facility Name
Bay Regional Medical Center
City
Bay City
State/Province
Michigan
ZIP/Postal Code
48708
Country
United States
Facility Name
Harper University Hospital
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201-2018
Country
United States
Facility Name
Henry Ford Hospital Heart & Vascular Institute
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48202
Country
United States
Facility Name
Borgess Medical Center
City
Kalamazoo
State/Province
Michigan
ZIP/Postal Code
49048
Country
United States
Facility Name
St. Joseph Mercy-PTCMI
City
Pontiac
State/Province
Michigan
ZIP/Postal Code
48341
Country
United States
Facility Name
William Beaumont Hospital
City
Royal Oak
State/Province
Michigan
ZIP/Postal Code
48073-6769
Country
United States
Facility Name
Covenant Medical Center
City
Saginaw
State/Province
Michigan
ZIP/Postal Code
48602
Country
United States
Facility Name
Great Lakes Heart & Vascular Institute, PC
City
Saint Joseph
State/Province
Michigan
ZIP/Postal Code
49085
Country
United States
Facility Name
Munson Medical Center
City
Traverse City
State/Province
Michigan
ZIP/Postal Code
49684
Country
United States
Facility Name
Beaumont Hospital Troy
City
Troy
State/Province
Michigan
ZIP/Postal Code
48085
Country
United States
Facility Name
Mayo Clinic - Saint Marys Hospital
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
Facility Name
Central Minnesota Heart Center at St. Cloud Hospital
City
Saint Cloud
State/Province
Minnesota
ZIP/Postal Code
56303
Country
United States
Facility Name
Hattiesburg Clinic
City
Hattiesburg
State/Province
Mississippi
ZIP/Postal Code
39401
Country
United States
Facility Name
Cardiology Associates Research LLC
City
Tupelo
State/Province
Mississippi
ZIP/Postal Code
38801
Country
United States
Facility Name
St. Luke's Hospital Mid America Heart Institute
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64111
Country
United States
Facility Name
Kansas City Heart Foundation
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64114
Country
United States
Facility Name
North Kansas City Hospital
City
North Kansas City
State/Province
Missouri
ZIP/Postal Code
64116
Country
United States
Facility Name
Washington University Hospital
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110-1093
Country
United States
Facility Name
St. Louis University Hospital
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Facility Name
St. John's Mercy Medical Center
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63141
Country
United States
Facility Name
St. John's Medical Institute
City
Springfield
State/Province
Missouri
ZIP/Postal Code
65807
Country
United States
Facility Name
Nebraska Heart Institute
City
Lincoln
State/Province
Nebraska
ZIP/Postal Code
68526
Country
United States
Facility Name
Alegent Health / Bergan Mercy Hospital
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68124
Country
United States
Facility Name
Creighton University
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68131
Country
United States
Facility Name
Catholic Medical Center
City
Manchester
State/Province
New Hampshire
ZIP/Postal Code
03102
Country
United States
Facility Name
Cooper University Hospital
City
Camden
State/Province
New Jersey
ZIP/Postal Code
08103
Country
United States
Facility Name
Cardiovascular Associates of the Delaware Valley, PA
City
Haddon Heights
State/Province
New Jersey
ZIP/Postal Code
08035
Country
United States
Facility Name
Hamilton Cardiology Associates
City
Hamilton
State/Province
New Jersey
ZIP/Postal Code
08690
Country
United States
Facility Name
Valley Hospital
City
Hawthorne
State/Province
New Jersey
ZIP/Postal Code
07506
Country
United States
Facility Name
UMDNJ - Robert Wood Johnson Medical School
City
New Brunswick
State/Province
New Jersey
ZIP/Postal Code
08901
Country
United States
Facility Name
St. Michaels Hospital
City
Newark
State/Province
New Jersey
ZIP/Postal Code
07102
Country
United States
Facility Name
Presbyterian Heart Group
City
Albuquerque
State/Province
New Mexico
ZIP/Postal Code
87106
Country
United States
Facility Name
SJH Cardiology Associates
City
Liverpool
State/Province
New York
ZIP/Postal Code
13088
Country
United States
Facility Name
Winthrop University Hospital
City
Mineola
State/Province
New York
ZIP/Postal Code
11501
Country
United States
Facility Name
Hudson Valley Heart Center
City
Poughkeepsie
State/Province
New York
ZIP/Postal Code
12601
Country
United States
Facility Name
Stony Brook University Medical Center
City
Stony Brook
State/Province
New York
ZIP/Postal Code
11794-8167
Country
United States
Facility Name
St. Elizabeth's Medical Center- NY
City
Utica
State/Province
New York
ZIP/Postal Code
13501
Country
United States
Facility Name
Westchester Medical Center
City
Valhalla
State/Province
New York
ZIP/Postal Code
10595
Country
United States
Facility Name
Asheville Cardiology Associates
City
Asheville
State/Province
North Carolina
ZIP/Postal Code
28802
Country
United States
Facility Name
Carolinas Medical Center
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28203
Country
United States
Facility Name
Carolina Heart Specialists
City
Gastonia
State/Province
North Carolina
ZIP/Postal Code
28054
Country
United States
Facility Name
Carolina Cardiology Associates
City
High Point
State/Province
North Carolina
ZIP/Postal Code
27262
Country
United States
Facility Name
Wake Heart Association
City
Raleigh
State/Province
North Carolina
ZIP/Postal Code
27610
Country
United States
Facility Name
Forsyth Medical Center
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27103
Country
United States
Facility Name
Wake Forest Health Sciences
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27157-1045
Country
United States
Facility Name
MeritCare Medical Center
City
Fargo
State/Province
North Dakota
ZIP/Postal Code
58122
Country
United States
Facility Name
Altru Health System
City
Grand Forks
State/Province
North Dakota
ZIP/Postal Code
58206
Country
United States
Facility Name
The Lindner Clinical Trial Center
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45219
Country
United States
Facility Name
Good Samaritan Hospital
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45220
Country
United States
Facility Name
University of Cincinnati Medical Center
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45267-0542
Country
United States
Facility Name
Riverside Methodist
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43214
Country
United States
Facility Name
Elyria Memorial Hospital
City
Elyria
State/Province
Ohio
ZIP/Postal Code
44035
Country
United States
Facility Name
Frederick C Smith Clinic dba Smith Clinic
City
Marion
State/Province
Ohio
ZIP/Postal Code
43302
Country
United States
Facility Name
Northwest Ohio Cardiology
City
Toledo
State/Province
Ohio
ZIP/Postal Code
43615
Country
United States
Facility Name
Midwest Regional Medical Center
City
Midwest City
State/Province
Oklahoma
ZIP/Postal Code
73110
Country
United States
Facility Name
University of Oklahoma Health Sciences Center
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
Facility Name
Oklahoma Foundation for CV Research
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73120
Country
United States
Facility Name
St. Vincent Hospital/ Providence Heart Hospital
City
Portland
State/Province
Oregon
ZIP/Postal Code
97225
Country
United States
Facility Name
Oregon Health & Sciences University Hospital
City
Portland
State/Province
Oregon
ZIP/Postal Code
97239-3098
Country
United States
Facility Name
Abington Memorial Hospital
City
Abington
State/Province
Pennsylvania
ZIP/Postal Code
19001
Country
United States
Facility Name
Chambersburg Hospital
City
Chambersburg
State/Province
Pennsylvania
ZIP/Postal Code
17201
Country
United States
Facility Name
Geisinger Clinic
City
Danville
State/Province
Pennsylvania
ZIP/Postal Code
17822
Country
United States
Facility Name
Doylestown Hospital
City
Doylestown
State/Province
Pennsylvania
ZIP/Postal Code
18901
Country
United States
Facility Name
Pinnacle Health Hospital
City
Harrisburg
State/Province
Pennsylvania
ZIP/Postal Code
17110
Country
United States
Facility Name
Conemaugh Memorial Medical Center
City
Johnstown
State/Province
Pennsylvania
ZIP/Postal Code
15905
Country
United States
Facility Name
UPMC Presbyterian Hospital
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
Facility Name
Donald Guthrie Foundation for Education and Research
City
Sayre
State/Province
Pennsylvania
ZIP/Postal Code
18840
Country
United States
Facility Name
Berks Cardiologists
City
Wyomissing
State/Province
Pennsylvania
ZIP/Postal Code
19610
Country
United States
Facility Name
York Hospital (PA)
City
York
State/Province
Pennsylvania
ZIP/Postal Code
17403
Country
United States
Facility Name
Rhode Island Hospital
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02903
Country
United States
Facility Name
Miriam Hospital
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02904
Country
United States
Facility Name
AnMed Health
City
Anderson
State/Province
South Carolina
ZIP/Postal Code
29621
Country
United States
Facility Name
Black Hills Research- Rapid City Regional
City
Rapid City
State/Province
South Dakota
ZIP/Postal Code
57701
Country
United States
Facility Name
North Central Heart Institute
City
Sioux Falls
State/Province
South Dakota
ZIP/Postal Code
57105
Country
United States
Facility Name
Sanford USD Medical Center
City
Sioux Falls
State/Province
South Dakota
ZIP/Postal Code
57117
Country
United States
Facility Name
Chattanooga Heart - East Third Street
City
Chattanooga
State/Province
Tennessee
ZIP/Postal Code
37404
Country
United States
Facility Name
Chattanooga Heart Institute
City
Chattanooga
State/Province
Tennessee
ZIP/Postal Code
37404
Country
United States
Facility Name
Centennial Heart Medical Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37203
Country
United States
Facility Name
Austin Heart
City
Austin
State/Province
Texas
ZIP/Postal Code
78705
Country
United States
Facility Name
Capital Cardiovascular Research Institute
City
Austin
State/Province
Texas
ZIP/Postal Code
78745
Country
United States
Facility Name
Texas Cardiovascular
City
Austin
State/Province
Texas
ZIP/Postal Code
78758
Country
United States
Facility Name
Veteran's Affairs Medical Center- Dallas
City
Dallas
State/Province
Texas
ZIP/Postal Code
75216
Country
United States
Facility Name
CRSTI Research
City
Dallas
State/Province
Texas
ZIP/Postal Code
75230
Country
United States
Facility Name
UT Southwestern Medical Center
City
Dallas
State/Province
Texas
ZIP/Postal Code
75390
Country
United States
Facility Name
Methodist DeBakey Heart & Vascular Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
North Dallas Research Associates
City
McKinney
State/Province
Texas
ZIP/Postal Code
75069
Country
United States
Facility Name
North Dallas Research Associate
City
McKinney
State/Province
Texas
ZIP/Postal Code
75069
Country
United States
Facility Name
The Heart Hospital / Baylor Plano
City
Plano
State/Province
Texas
ZIP/Postal Code
75093
Country
United States
Facility Name
Scott and White Healthcare - Round Rock
City
Round Rock
State/Province
Texas
ZIP/Postal Code
78665
Country
United States
Facility Name
TexSan Heart Hospital
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States
Facility Name
Mother Frances Hospital
City
Tyler
State/Province
Texas
ZIP/Postal Code
75701
Country
United States
Facility Name
Providence Healthcare Network
City
Waco
State/Province
Texas
ZIP/Postal Code
76712
Country
United States
Facility Name
Intermountain Medical Center
City
Murray
State/Province
Utah
ZIP/Postal Code
84157-7000
Country
United States
Facility Name
University of Virginia
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22908
Country
United States
Facility Name
Rockingham Memorial Hospital
City
Harrisonburg
State/Province
Virginia
ZIP/Postal Code
22801
Country
United States
Facility Name
Lynchburg General Hospital
City
Lynchburg
State/Province
Virginia
ZIP/Postal Code
24501
Country
United States
Facility Name
Sentara, Norfolk General Hospital
City
Norfolk
State/Province
Virginia
ZIP/Postal Code
23507
Country
United States
Facility Name
Carilion Clinic
City
Roanoke
State/Province
Virginia
ZIP/Postal Code
24014
Country
United States
Facility Name
Cardiovascular Associates, Ltd.
City
Virginia Beach
State/Province
Virginia
ZIP/Postal Code
23454
Country
United States
Facility Name
Winchester Medical Center
City
Winchester
State/Province
Virginia
ZIP/Postal Code
22601
Country
United States
Facility Name
Providence St. Peter Hospital
City
Olympia
State/Province
Washington
ZIP/Postal Code
98506
Country
United States
Facility Name
University of Washington
City
Seattle
State/Province
Washington
ZIP/Postal Code
98195-8422
Country
United States
Facility Name
Inland Cardiology Associates
City
Spokane
State/Province
Washington
ZIP/Postal Code
99204
Country
United States
Facility Name
Sacred Heart Medical Center
City
Spokane
State/Province
Washington
ZIP/Postal Code
99204
Country
United States
Facility Name
Aurora St. Luke's Medical Center
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53215
Country
United States
Facility Name
CaRE Foundation, Inc.
City
Wausau
State/Province
Wisconsin
ZIP/Postal Code
54401
Country
United States
Facility Name
St. Vincents Hospital Sydney
City
Darlinghurst
State/Province
New South Wales
ZIP/Postal Code
2010
Country
Australia
Facility Name
Prince of Wales Eastern Heart
City
Randwick
State/Province
New South Wales
ZIP/Postal Code
2031
Country
Australia
Facility Name
Royal Adelaide Hospital
City
Adelaide
State/Province
South Australia
ZIP/Postal Code
5000
Country
Australia
Facility Name
The Alfred Hospital
City
Prahran
State/Province
Victoria
ZIP/Postal Code
3004
Country
Australia
Facility Name
Fremantle Hospital
City
Fremantle
State/Province
Western Australia
ZIP/Postal Code
6160
Country
Australia
Facility Name
The Mount Hospital
City
Nedlands
State/Province
Western Australia
ZIP/Postal Code
6009
Country
Australia
Facility Name
Royal Perth Hospital
City
Perth
State/Province
Western Australia
ZIP/Postal Code
6000
Country
Australia
Facility Name
Monash Heart
City
Clayton
ZIP/Postal Code
3168
Country
Australia
Facility Name
St Vincents Hospital Melbourne
City
Fitzroy
ZIP/Postal Code
3065
Country
Australia
Facility Name
Fakultni nemocnice Hradec Kralove
City
Hradec Kralove
ZIP/Postal Code
500 05
Country
Czechia
Facility Name
Krajska karlovarska nemocnice a.s.
City
Karlovy Vary
ZIP/Postal Code
360 66
Country
Czechia
Facility Name
Centrum pro choroby srdce a cev
City
Kromeriz
ZIP/Postal Code
767 01
Country
Czechia
Facility Name
Mestska nemocnice Ostrava
City
Ostrava
ZIP/Postal Code
701 00
Country
Czechia
Facility Name
Krajska nemocnice T. Bati a.s.
City
Zlin
ZIP/Postal Code
76275
Country
Czechia
Facility Name
Centre Hospitalier Saint Louis
City
La Rochelle
ZIP/Postal Code
17000
Country
France
Facility Name
Hospital Saint Philibert
City
Lomme
ZIP/Postal Code
59462
Country
France
Facility Name
Nouvelles Cliniques Nantaises
City
Nantes
ZIP/Postal Code
44277
Country
France
Facility Name
Clinique les Franciscaines
City
Nimes
ZIP/Postal Code
30000
Country
France
Facility Name
Hopital Bichat
City
Paris
ZIP/Postal Code
75018
Country
France
Facility Name
Groupe Hospitalier Sud
City
Pessac
ZIP/Postal Code
33604
Country
France
Facility Name
CH Chatiliez Tourcoing
City
Tourcoing
ZIP/Postal Code
59208
Country
France
Facility Name
Helios Klinikum Emil von Behring
City
Berlin
State/Province
BE
ZIP/Postal Code
1
Country
Germany
Facility Name
Universitaetsklinikum Schleswig-Holstein - PS
City
Luebeck
State/Province
SH
ZIP/Postal Code
23538
Country
Germany
Facility Name
Vivantes Klinikum im Friedrichshain
City
Berlin
ZIP/Postal Code
10249
Country
Germany
Facility Name
Vivantes-Klinikum Neukoelin
City
Berlin
ZIP/Postal Code
12351
Country
Germany
Facility Name
Vivantes-Klinikum Neukoelln
City
Berlin
ZIP/Postal Code
13437
Country
Germany
Facility Name
Vivantes-Humboldt Klinikum
City
Berlin
ZIP/Postal Code
13509
Country
Germany
Facility Name
Elbe-Kliniken Stade-Buxtehude GmbH
City
Buxtehude
ZIP/Postal Code
21614
Country
Germany
Facility Name
Universitaetsklinikum Dresden
City
Dresden
ZIP/Postal Code
01307
Country
Germany
Facility Name
Asklepios Klinik St. Georg
City
Hamburg
ZIP/Postal Code
20099
Country
Germany
Facility Name
Herzzentrum Leipzig GmbH
City
Leipzig
ZIP/Postal Code
4289
Country
Germany
Facility Name
Elbe-Kliniken Stade-Buxtehude GmbH
City
Stade
ZIP/Postal Code
21682
Country
Germany
Facility Name
Gottsegen Gyorgy Orszagos Kardiologiai Intezet
City
Budapest
ZIP/Postal Code
1096
Country
Hungary
Facility Name
Josa Andras Oktato Korhaz Nonprofit Kft
City
Nyiregyhaza
ZIP/Postal Code
4400
Country
Hungary
Facility Name
Pecsi Tudomanyegyetem Klinikai Kozpont
City
Pecs
Country
Hungary
Facility Name
Szegedi Tudomanyegyetem Szent-Gyorgyi Klinikai Kozpont
City
Szeged
ZIP/Postal Code
6720
Country
Hungary
Facility Name
Zala Megyei Korhaz
City
Zalaegerszeg
ZIP/Postal Code
8900
Country
Hungary
Facility Name
Mercy Angiography
City
Epsom
State/Province
Auckland
ZIP/Postal Code
00000
Country
New Zealand
Facility Name
North Shore Hospital
City
Auckland
ZIP/Postal Code
0622
Country
New Zealand
Facility Name
Ascot Hospital
City
Auckland
Country
New Zealand
Facility Name
Middlemore Hospital
City
Auckland
Country
New Zealand
Facility Name
Christchurch Hospital
City
Christchurch
ZIP/Postal Code
8001
Country
New Zealand
Facility Name
Waikato Hospital
City
Hamilton
ZIP/Postal Code
3240
Country
New Zealand
Facility Name
Nelson Hospital
City
Nelson
Country
New Zealand
Facility Name
Wellington Hospital
City
Wellington
ZIP/Postal Code
6021
Country
New Zealand
Facility Name
Wakefield Hospital
City
Wellington
ZIP/Postal Code
6039
Country
New Zealand
Facility Name
Uniwersyteck Szpital Klin. w Bialymstoku
City
Bialystok
ZIP/Postal Code
15-276
Country
Poland
Facility Name
Wielospecj. Szpital Miejski im.dr.E.Warminskiego-SPZOZ
City
Bydgoszcz
ZIP/Postal Code
85-826
Country
Poland
Facility Name
NZOZ Centrum Medyczne Beluga-Med
City
Krakow
ZIP/Postal Code
30-069
Country
Poland
Facility Name
Szpital Uniwersytecki w Krakowie
City
Krakow
ZIP/Postal Code
31-501
Country
Poland
Facility Name
SPSK nr 2 Pomorskiej Akademii Medycznej w Szczecinie
City
Szczecin
ZIP/Postal Code
70-111
Country
Poland
Facility Name
Polsko-Amerykanskie Kliniki Serca.American Heart of Poland S
City
Ustron
ZIP/Postal Code
43-450
Country
Poland
Facility Name
Instytut Kardiologii im. Kardynala St. Wyszynskiego
City
Warszawa
ZIP/Postal Code
04-637
Country
Poland
Facility Name
Centrul Clinic de Urgenta de Boli Cardiovasculare al Armatei
City
Bucuresti
ZIP/Postal Code
10242
Country
Romania
Facility Name
Spitalul Clinic de Urgenta Bucuresti
City
Bucuresti
ZIP/Postal Code
14461
Country
Romania
Facility Name
Inst. Urgenta Boli Cardiovasculare Prof. Dr. C.C. Iliescu
City
Bucuresti
ZIP/Postal Code
22328
Country
Romania
Facility Name
Institutul de Urgenta pentru Boli Cardiovasculare Prof. Dr.
City
Bucuresti
ZIP/Postal Code
22328
Country
Romania
Facility Name
Spitalul Clinic Universitar de Urgenta Bucuresti
City
Bucuresti
ZIP/Postal Code
50098
Country
Romania
Facility Name
Institutul Inimii Niculae Stancioiu Cluj-Napoca
City
Cluj-Napoca
ZIP/Postal Code
400001
Country
Romania
Facility Name
Institutul de Boli Cardiovasculare si Transplant Targu Mures
City
Targu Mures
ZIP/Postal Code
540136
Country
Romania
Facility Name
Wycombe General Hospital
City
High Wycombe
State/Province
Bucks
ZIP/Postal Code
HP11 2TT
Country
United Kingdom
Facility Name
Papworth Hospital
City
Cambridge
State/Province
Cambs
ZIP/Postal Code
CB3 8RE
Country
United Kingdom
Facility Name
Torbay hospital
City
Torquay
State/Province
Devon
ZIP/Postal Code
TQ2 7AA
Country
United Kingdom
Facility Name
Royal Bournemouth General Hospital
City
Bournemouth
State/Province
Dorset
ZIP/Postal Code
BH7 7DW
Country
United Kingdom
Facility Name
Basildon University Hospital
City
Basildon
State/Province
Essex
ZIP/Postal Code
SS16 5NL
Country
United Kingdom
Facility Name
Barnet Hospital
City
Barnet
State/Province
Herts
ZIP/Postal Code
EN5 3DJ
Country
United Kingdom
Facility Name
James Cook Hospital
City
Middlesborough
State/Province
N York
ZIP/Postal Code
TS4 3BW
Country
United Kingdom
Facility Name
Ninewells Hospital
City
Dundee
State/Province
Scotland
ZIP/Postal Code
DD1 9SY
Country
United Kingdom
Facility Name
Weston General Hospital
City
Weston Super Mare
State/Province
Somerset
ZIP/Postal Code
BS23 4TQ
Country
United Kingdom
Facility Name
Golden Jubilee National Hospital
City
Glasgow
State/Province
Strath
ZIP/Postal Code
F81 4HX
Country
United Kingdom
Facility Name
St Peter's Hospital
City
Chertsey
ZIP/Postal Code
KT16 OPZ
Country
United Kingdom
Facility Name
University Hospital of Coventry and Warwickshire
City
Coventry
ZIP/Postal Code
CV2 2DX
Country
United Kingdom
Facility Name
Ninewells Hospital
City
Dundee
ZIP/Postal Code
DD1 9SY
Country
United Kingdom
Facility Name
Royal Infirmary of Edinburgh
City
Edinburgh
ZIP/Postal Code
EH16 4SA
Country
United Kingdom
Facility Name
University Hospital of Leicester Glenfield Hospital
City
Leicester
ZIP/Postal Code
LE3 9QP
Country
United Kingdom
Facility Name
The London Chest Hospital
City
London
ZIP/Postal Code
E2 9JX
Country
United Kingdom
Facility Name
Freeman Hospital
City
Newcastle
ZIP/Postal Code
NE7 7AW
Country
United Kingdom
Facility Name
Derriford Hospital
City
Plymouth
ZIP/Postal Code
PL6 8DH
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
32683645
Citation
Berg DD, Yeh RW, Mauri L, Morrow DA, Kereiakes DJ, Cutlip DE, Gao Q, Jarolim P, Michelson AD, Frelinger AL 3rd, Cange AL, Sabatine MS, O'Donoghue ML. Biomarkers of platelet activation and cardiovascular risk in the DAPT trial. J Thromb Thrombolysis. 2021 Apr;51(3):675-681. doi: 10.1007/s11239-020-02221-5.
Results Reference
derived
PubMed Identifier
31653353
Citation
Stefanescu Schmidt AC, Steg PG, Yeh RW, Kereiakes DJ, Tanguay JF, Hsieh WH, Massaro JM, Mauri L, Cutlip DE; DAPT Investigators. Interruption of Dual Antiplatelet Therapy Within Six Months After Coronary Stents (from the Dual Antiplatelet Therapy Study). Am J Cardiol. 2019 Dec 15;124(12):1813-1820. doi: 10.1016/j.amjcard.2019.09.006. Epub 2019 Sep 26.
Results Reference
derived
PubMed Identifier
30354781
Citation
Berry NC, Kereiakes DJ, Yeh RW, Steg PG, Cutlip DE, Jacobs AK, Abbott JD, Hsieh WH, Massaro JM, Mauri L; DAPT Study Investigators. Benefit and Risk of Prolonged DAPT After Coronary Stenting in Women. Circ Cardiovasc Interv. 2018 Aug;11(8):e005308. doi: 10.1161/CIRCINTERVENTIONS.117.005308.
Results Reference
derived
PubMed Identifier
29073947
Citation
Yeh RW, Kereiakes DJ, Steg PG, Cutlip DE, Croce KJ, Massaro JM, Mauri L; DAPT Study Investigators. Lesion Complexity and Outcomes of Extended Dual Antiplatelet Therapy After Percutaneous Coronary Intervention. J Am Coll Cardiol. 2017 Oct 31;70(18):2213-2223. doi: 10.1016/j.jacc.2017.09.011.
Results Reference
derived
PubMed Identifier
28297015
Citation
Secemsky EA, Yeh RW, Kereiakes DJ, Cutlip DE, Cohen DJ, Steg PG, Cannon CP, Apruzzese PK, D'Agostino RB Sr, Massaro JM, Mauri L; Dual Antiplatelet Therapy (DAPT) Study Investigators. Mortality Following Cardiovascular and Bleeding Events Occurring Beyond 1 Year After Coronary Stenting: A Secondary Analysis of the Dual Antiplatelet Therapy (DAPT) Study. JAMA Cardiol. 2017 May 1;2(5):478-487. doi: 10.1001/jamacardio.2017.0063.
Results Reference
derived
PubMed Identifier
28228427
Citation
Stefanescu Schmidt AC, Kereiakes DJ, Cutlip DE, Yeh RW, D'Agostino RB Sr, Massaro JM, Hsieh WH, Mauri L; DAPT Investigators. Myocardial Infarction Risk After Discontinuation of Thienopyridine Therapy in the Randomized DAPT Study (Dual Antiplatelet Therapy). Circulation. 2017 May 2;135(18):1720-1732. doi: 10.1161/CIRCULATIONAHA.116.024835. Epub 2017 Feb 22.
Results Reference
derived
PubMed Identifier
27576774
Citation
Resor CD, Nathan A, Kereiakes DJ, Yeh RW, Massaro JM, Cutlip DE, Gabriel Steg P, Hsieh WH, Mauri L; Dual Antiplatelet Therapy Study Investigators. Impact of Optimal Medical Therapy in the Dual Antiplatelet Therapy Study. Circulation. 2016 Oct 4;134(14):989-998. doi: 10.1161/CIRCULATIONAHA.116.024531. Epub 2016 Aug 30.
Results Reference
derived
PubMed Identifier
27046159
Citation
Kereiakes DJ, Yeh RW, Massaro JM, Cutlip DE, Steg PG, Wiviott SD, Mauri L; DAPT Study Investigators. DAPT Score Utility for Risk Prediction in Patients With or Without Previous Myocardial Infarction. J Am Coll Cardiol. 2016 May 31;67(21):2492-502. doi: 10.1016/j.jacc.2016.03.485. Epub 2016 Apr 1.
Results Reference
derived
PubMed Identifier
27022822
Citation
Yeh RW, Secemsky EA, Kereiakes DJ, Normand SL, Gershlick AH, Cohen DJ, Spertus JA, Steg PG, Cutlip DE, Rinaldi MJ, Camenzind E, Wijns W, Apruzzese PK, Song Y, Massaro JM, Mauri L; DAPT Study Investigators. Development and Validation of a Prediction Rule for Benefit and Harm of Dual Antiplatelet Therapy Beyond 1 Year After Percutaneous Coronary Intervention. JAMA. 2016 Apr 26;315(16):1735-49. doi: 10.1001/jama.2016.3775. Erratum In: JAMA. 2016 Jul 19;316(3):350. JAMA. 2016 Jul 19;316(3):350.
Results Reference
derived
PubMed Identifier
26994121
Citation
Meredith IT, Tanguay JF, Kereiakes DJ, Cutlip DE, Yeh RW, Garratt KN, Lee DP, Steg PG, Weaver WD, Holmes DR Jr, Brindis RG, Trebacz J, Massaro JM, Hsieh WH, Mauri L; DAPT Study Investigators. Diabetes Mellitus and Prevention of Late Myocardial Infarction After Coronary Stenting in the Randomized Dual Antiplatelet Therapy Study. Circulation. 2016 May 3;133(18):1772-82. doi: 10.1161/CIRCULATIONAHA.115.016783. Epub 2016 Mar 18. Erratum In: Circulation. 2016 May 31;133(22):e671.
Results Reference
derived
PubMed Identifier
26793956
Citation
Hermiller JB, Krucoff MW, Kereiakes DJ, Windecker S, Steg PG, Yeh RW, Cohen DJ, Cutlip DE, Massaro JM, Hsieh WH, Mauri L; DAPT Study Investigators. Benefits and Risks of Extended Dual Antiplatelet Therapy After Everolimus-Eluting Stents. JACC Cardiovasc Interv. 2016 Jan 25;9(2):138-47. doi: 10.1016/j.jcin.2015.10.001.
Results Reference
derived
PubMed Identifier
26586780
Citation
Mauri L, Elmariah S, Yeh RW, Cutlip DE, Steg PG, Windecker S, Wiviott SD, Cohen DJ, Massaro JM, D'Agostino RB Sr, Braunwald E, Kereiakes DJ; DAPT Study Investigators. Causes of late mortality with dual antiplatelet therapy after coronary stents. Eur Heart J. 2016 Jan 21;37(4):378-85. doi: 10.1093/eurheartj/ehv614. Epub 2015 Nov 18.
Results Reference
derived
PubMed Identifier
26493248
Citation
Kereiakes DJ, Yeh RW, Massaro JM, Driscoll-Shempp P, Cutlip DE, Steg PG, Gershlick AH, Darius H, Meredith IT, Ormiston J, Tanguay JF, Windecker S, Garratt KN, Kandzari DE, Lee DP, Simon DI, Iancu AC, Trebacz J, Mauri L; DAPT Study Investigators. Stent Thrombosis in Drug-Eluting or Bare-Metal Stents in Patients Receiving Dual Antiplatelet Therapy. JACC Cardiovasc Interv. 2015 Oct;8(12):1552-62. doi: 10.1016/j.jcin.2015.05.026. Erratum In: JACC Cardiovasc Interv. 2015 Dec 21;8(14):1913.
Results Reference
derived
PubMed Identifier
25787199
Citation
Yeh RW, Kereiakes DJ, Steg PG, Windecker S, Rinaldi MJ, Gershlick AH, Cutlip DE, Cohen DJ, Tanguay JF, Jacobs A, Wiviott SD, Massaro JM, Iancu AC, Mauri L; DAPT Study Investigators. Benefits and Risks of Extended Duration Dual Antiplatelet Therapy After PCI in Patients With and Without Acute Myocardial Infarction. J Am Coll Cardiol. 2015 May 26;65(20):2211-21. doi: 10.1016/j.jacc.2015.03.003. Epub 2015 Mar 15.
Results Reference
derived
PubMed Identifier
25781440
Citation
Kereiakes DJ, Yeh RW, Massaro JM, Driscoll-Shempp P, Cutlip DE, Steg PG, Gershlick AH, Darius H, Meredith IT, Ormiston J, Tanguay JF, Windecker S, Garratt KN, Kandzari DE, Lee DP, Simon DI, Iancu AC, Trebacz J, Mauri L; Dual Antiplatelet Therapy (DAPT) Study Investigators. Antiplatelet therapy duration following bare metal or drug-eluting coronary stents: the dual antiplatelet therapy randomized clinical trial. JAMA. 2015 Mar 17;313(11):1113-21. doi: 10.1001/jama.2015.1671. Erratum In: JAMA. 2015 Jun 2;313(21):2185. JAMA. 2016 Jul 5;316(1):105. JAMA. 2016 Jul 5;316(1):105.
Results Reference
derived
PubMed Identifier
25399847
Citation
Yeh RW, Czarny MJ, Normand SL, Kereiakes DJ, Holmes DR Jr, Brindis RG, Weaver WD, Rumsfeld JS, Roe MT, Kim S, Driscoll-Shempp P, Mauri L. Evaluating the generalizability of a large streamlined cardiovascular trial: comparing hospitals and patients in the dual antiplatelet therapy study versus the National Cardiovascular Data Registry. Circ Cardiovasc Qual Outcomes. 2015 Jan;8(1):96-102. doi: 10.1161/CIRCOUTCOMES.114.001239. Epub 2014 Nov 16.
Results Reference
derived
PubMed Identifier
25399658
Citation
Mauri L, Kereiakes DJ, Yeh RW, Driscoll-Shempp P, Cutlip DE, Steg PG, Normand SL, Braunwald E, Wiviott SD, Cohen DJ, Holmes DR Jr, Krucoff MW, Hermiller J, Dauerman HL, Simon DI, Kandzari DE, Garratt KN, Lee DP, Pow TK, Ver Lee P, Rinaldi MJ, Massaro JM; DAPT Study Investigators. Twelve or 30 months of dual antiplatelet therapy after drug-eluting stents. N Engl J Med. 2014 Dec 4;371(23):2155-66. doi: 10.1056/NEJMoa1409312. Epub 2014 Nov 16.
Results Reference
derived
PubMed Identifier
24332248
Citation
Matteau A, Yeh RW, Kereiakes D, Orav EJ, Massaro J, Steg PG, Normand SL, Cutlip DE, Mauri L. Frequency of the use of low- versus high-dose aspirin in dual antiplatelet therapy after percutaneous coronary intervention (from the Dual Antiplatelet Therapy study). Am J Cardiol. 2014 Apr 1;113(7):1146-52. doi: 10.1016/j.amjcard.2013.10.015. Epub 2013 Nov 8.
Results Reference
derived
PubMed Identifier
21146655
Citation
Mauri L, Kereiakes DJ, Normand SL, Wiviott SD, Cohen DJ, Holmes DR, Bangalore S, Cutlip DE, Pencina M, Massaro JM. Rationale and design of the dual antiplatelet therapy study, a prospective, multicenter, randomized, double-blind trial to assess the effectiveness and safety of 12 versus 30 months of dual antiplatelet therapy in subjects undergoing percutaneous coronary intervention with either drug-eluting stent or bare metal stent placement for the treatment of coronary artery lesions. Am Heart J. 2010 Dec;160(6):1035-41, 1041.e1. doi: 10.1016/j.ahj.2010.07.038.
Results Reference
derived

Learn more about this trial

The Dual Antiplatelet Therapy Study (DAPT Study)

We'll reach out to this number within 24 hrs