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Triple Therapy in Patients on Oral Anticoagulation After Drug Eluting Stent Implantation (ISAR-TRIPLE)

Primary Purpose

Coronary Artery Disease, Atrial Fibrillation

Status
Unknown status
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
aspirin
clopidogrel
oral anticoagulation
Sponsored by
Deutsches Herzzentrum Muenchen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring aspirin, clopidogrel, oral anticoagulation, warfarin, drug eluting stent, phenprocoumon

Eligibility Criteria

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

Key Inclusion Criteria:

  1. Patients with an indication for oral anticoagulation and a DES implantation.
  2. Informed, written consent by the patient or her/his legally-authorized representative for participation in the study.

Key Exclusion Criteria:

  1. Age ≤18 years
  2. Previous stent thrombosis
  3. DES in left main

Sites / Locations

  • Aarhus University Hospital
  • Deutsches Herzzentrum München
  • 1. Medizinische Klinik, Klinikum rechts der Isar

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Short triple

Long triple

Arm Description

6 weeks triple therapy

6 months triple therapy

Outcomes

Primary Outcome Measures

Composite of death, myocardial infarction, definite stent thrombosis, stroke or major bleeding.

Secondary Outcome Measures

Ischemic complications (composite of cardiac death, myocardial infarction, stent thrombosis or ischemic stroke)
Bleeding complications (Major bleeding)

Full Information

First Posted
October 20, 2008
Last Updated
August 29, 2016
Sponsor
Deutsches Herzzentrum Muenchen
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1. Study Identification

Unique Protocol Identification Number
NCT00776633
Brief Title
Triple Therapy in Patients on Oral Anticoagulation After Drug Eluting Stent Implantation
Acronym
ISAR-TRIPLE
Official Title
Intracoronary Stenting and Antithrombotic Regimen: Testing of a Six-week Versus a Six-month Clopidogrel Treatment Regimen in Patients With Concomitant Aspirin and Oral Anticoagulant Therapy Following Drug-eluting Stenting
Study Type
Interventional

2. Study Status

Record Verification Date
August 2014
Overall Recruitment Status
Unknown status
Study Start Date
September 2008 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
September 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Deutsches Herzzentrum Muenchen

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators hypothesize that reducing the duration of clopidogrel therapy from 6 months to 6 weeks after DES implantation is associated with improved clinical outcomes in patients on ASA and an oral anticoagulant.
Detailed Description
The introduction of drug-eluting stents (DES) was associated not only with a widening of the indication for percutaneous coronary intervention (PCI) but also with longer antithrombotic therapy duration. Dual antiplatelet therapy with ASA and a thienopyridine is very efficient in preventing adverse events after coronary stenting but it is inferior to oral anticoagulation (OAC) to reduce the risk of stroke in patients with atrial fibrillation. OAC is also superior to antiplatelet therapy in patients with mechanical heart valves and the therapy of choice for the treatment of deep vein thrombosis and pulmonary embolism. OAC is also administered for left ventricular thrombi and low ejection fraction. There is an increasing number of patients undergoing coronary stenting who are in need of life-long anticoagulation therapy and would therefore require a triple therapy consisting of aspirin, clopidogrel and oral anticoagulation. As oral anticoagulation and antithrombotic therapy impair primary and secondary hemostasis there are concerns that adding warfarin to dual antiplatelet therapy might cause increased bleeding rates. Several studies have retrospectively assessed efficacy and safety in patients receiving a triple therapy with various results: major bleeding rates varied from 3,1%-14,9% with total bleeding rates up to 27,5%. Prospective randomized data on this topic are not available. Therefore the aim of this study is to compare a 6 week versus a 6 month triple therapy after DES implantation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Atrial Fibrillation
Keywords
aspirin, clopidogrel, oral anticoagulation, warfarin, drug eluting stent, phenprocoumon

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
614 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Short triple
Arm Type
Experimental
Arm Description
6 weeks triple therapy
Arm Title
Long triple
Arm Type
Active Comparator
Arm Description
6 months triple therapy
Intervention Type
Drug
Intervention Name(s)
aspirin
Intervention Description
6 weeks triple therapy with aspirin, clopidogrel and oral anticoagulation
Intervention Type
Drug
Intervention Name(s)
clopidogrel
Intervention Description
6 months triple therapy with aspirin, clopidogrel and oral anticoagulation
Intervention Type
Drug
Intervention Name(s)
oral anticoagulation
Primary Outcome Measure Information:
Title
Composite of death, myocardial infarction, definite stent thrombosis, stroke or major bleeding.
Time Frame
9 months
Secondary Outcome Measure Information:
Title
Ischemic complications (composite of cardiac death, myocardial infarction, stent thrombosis or ischemic stroke)
Time Frame
9 months
Title
Bleeding complications (Major bleeding)
Time Frame
9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Key Inclusion Criteria: Patients with an indication for oral anticoagulation and a DES implantation. Informed, written consent by the patient or her/his legally-authorized representative for participation in the study. Key Exclusion Criteria: Age ≤18 years Previous stent thrombosis DES in left main
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adnan Kastrati, MD
Organizational Affiliation
Deutsches Herzzentum München
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Stefanie Schulz, MD
Organizational Affiliation
Deutsches Herzzentrum Muenchen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Aarhus University Hospital
City
Aarhus
ZIP/Postal Code
8200
Country
Denmark
Facility Name
Deutsches Herzzentrum München
City
Munich
ZIP/Postal Code
80636
Country
Germany
Facility Name
1. Medizinische Klinik, Klinikum rechts der Isar
City
München
ZIP/Postal Code
81675
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
18608125
Citation
Rubboli A, Halperin JL, Airaksinen KE, Buerke M, Eeckhout E, Freedman SB, Gershlick AH, Schlitt A, Tse HF, Verheugt FW, Lip GY. Antithrombotic therapy in patients treated with oral anticoagulation undergoing coronary artery stenting. An expert consensus document with focus on atrial fibrillation. Ann Med. 2008;40(6):428-36. doi: 10.1080/07853890802089786.
Results Reference
background
PubMed Identifier
8598866
Citation
Schomig A, Neumann FJ, Kastrati A, Schuhlen H, Blasini R, Hadamitzky M, Walter H, Zitzmann-Roth EM, Richardt G, Alt E, Schmitt C, Ulm K. A randomized comparison of antiplatelet and anticoagulant therapy after the placement of coronary-artery stents. N Engl J Med. 1996 Apr 25;334(17):1084-9. doi: 10.1056/NEJM199604253341702.
Results Reference
background
PubMed Identifier
25908066
Citation
Fiedler KA, Maeng M, Mehilli J, Schulz-Schupke S, Byrne RA, Sibbing D, Hoppmann P, Schneider S, Fusaro M, Ott I, Kristensen SD, Ibrahim T, Massberg S, Schunkert H, Laugwitz KL, Kastrati A, Sarafoff N. Duration of Triple Therapy in Patients Requiring Oral Anticoagulation After Drug-Eluting Stent Implantation: The ISAR-TRIPLE Trial. J Am Coll Cardiol. 2015 Apr 28;65(16):1619-1629. doi: 10.1016/j.jacc.2015.02.050.
Results Reference
derived
PubMed Identifier
24655693
Citation
Fiedler KA, Byrne RA, Schulz S, Sibbing D, Mehilli J, Ibrahim T, Maeng M, Laugwitz KL, Kastrati A, Sarafoff N. Rationale and design of The Intracoronary Stenting and Antithrombotic Regimen-Testing of a six-week versus a six-month clopidogrel treatment Regimen In Patients with concomitant aspirin and oraL anticoagulant therapy following drug-Eluting stenting (ISAR-TRIPLE) study. Am Heart J. 2014 Apr;167(4):459-465.e1. doi: 10.1016/j.ahj.2014.01.005. Epub 2014 Jan 14.
Results Reference
derived

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Triple Therapy in Patients on Oral Anticoagulation After Drug Eluting Stent Implantation

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