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EArly Discharge After Transradial Stenting of CoronarY Arteries in High-Risk Patients of Bleeding (EASY-B2B)

Primary Purpose

Coronary Artery Disease

Status
Unknown status
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Bivalirudin
Heparin
Sponsored by
Laval University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring Coronary artery stenting, transradial, intracoronary

Eligibility Criteria

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

Inclusion Criteria:

  • At least two of the following additional criteria
  • At least 70 yrs old
  • Female gender
  • Diabetes
  • Creatinine clearance <60mL/min
  • History of gastro-intestinal or other organ bleeding
  • Baseline anemia
  • Current treatment with glycoproteins IIb-IIIa inhibitors

Exclusion Criteria:

  • Intolerance or allergy to ASA, clopidogrel or ticlopidine precluding treatment for 12 months
  • Concurrent participation in other investigational study
  • Femoral sheath (artery)

Sites / Locations

  • Quebec Heart-Lung InstituteRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Bivalirudin

Heparin

Arm Description

Standard practice: 0.75mg/kg + infusion 1.75mg/kg/h

70 U/kg or standard practice

Outcomes

Primary Outcome Measures

Major bleeding and Mace
The primary end-points will be 1) the incidence of major bleeding (Replace-2 criteria) at hospital discharge and 2) the incidence of 24h post-PCI anemia (WHO criteria)

Secondary Outcome Measures

EFFICACY and SAFETY PARAMETERS
The composite of death, MI (def 1 : Tn-t > 0.1 and def 2 : CK-MB > 30μg/l), urgent revascularization and major bleeding at 30 days post-PCI. The incidence of ARC-defined stent thrombosis at 30 days. The incidence of access-site hematoma according to EASY scale. The incidence of radial artery occlusion at hospital discharge according to echo-doppler evaluation

Full Information

First Posted
March 9, 2010
Last Updated
January 29, 2018
Sponsor
Laval University
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1. Study Identification

Unique Protocol Identification Number
NCT01084993
Brief Title
EArly Discharge After Transradial Stenting of CoronarY Arteries in High-Risk Patients of Bleeding
Acronym
EASY-B2B
Official Title
EArly Discharge After Transradial Stenting of CoronarY Arteries in High-Risk Patients of Bleeding: Bivalirudin to Reduce Bleeding EASY-B2B Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Unknown status
Study Start Date
March 2010 (undefined)
Primary Completion Date
September 2018 (Anticipated)
Study Completion Date
January 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Laval University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
RATIONALE: Transradial coronary stenting is associated with less risk of access site complications and bleeding compared to femoral approach. Major bleeding post-PCI is a strong independent predictor of mortality and MACE. Depending of the antithrombotic regimen and access-site used, bleeding related to access-site represents 50-80% of the cases. Whereas transradial approach minimizes the risks of access-site bleeding, it has no impact on non-access site bleeding. Peri-procedural anemia is also an independent predictor of mortality and MACE. With femoral approach, bivalirudin compared to heparin ± glycoproteins IIb-IIIa has been associated with a significant reduction in access-site and non-access site related bleeding. In a post-hoc analysis of patients treated by transradial approach in ACUITY, there was a trend for non-access site bleeding (organ bleeding) with bivalirudin compared to heparin ± glycoproteins IIb-IIIa. HYPOTHESES: In patients at high-risk of peri-procedural bleeding, bivalirudin ± glycoproteins IIb-IIIa reduces the risk of bleeding compared to heparin ± glycoproteins IIb-IIIa. In patients at high-risk of bleeding and undergoing transradial PCI, bivalirudin significantly reduces the incidence of non-access site bleeding and peri-procedural anemia.
Detailed Description
OBJECTIVES: The primary objective is to compare the incidence of major bleeding and anemia 24h post-PCI in patients at high-risk of bleeding after transradial PCI with heparin or bivalirudin.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease
Keywords
Coronary artery stenting, transradial, intracoronary

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Bivalirudin
Arm Type
Active Comparator
Arm Description
Standard practice: 0.75mg/kg + infusion 1.75mg/kg/h
Arm Title
Heparin
Arm Type
Active Comparator
Arm Description
70 U/kg or standard practice
Intervention Type
Drug
Intervention Name(s)
Bivalirudin
Other Intervention Name(s)
Angiomax
Intervention Description
Standard practice: 0.75mg/kg + infusion 1.75mg/kg/h
Intervention Type
Drug
Intervention Name(s)
Heparin
Intervention Description
70 U/kg
Primary Outcome Measure Information:
Title
Major bleeding and Mace
Description
The primary end-points will be 1) the incidence of major bleeding (Replace-2 criteria) at hospital discharge and 2) the incidence of 24h post-PCI anemia (WHO criteria)
Time Frame
24h post-PCI and Discharge
Secondary Outcome Measure Information:
Title
EFFICACY and SAFETY PARAMETERS
Description
The composite of death, MI (def 1 : Tn-t > 0.1 and def 2 : CK-MB > 30μg/l), urgent revascularization and major bleeding at 30 days post-PCI. The incidence of ARC-defined stent thrombosis at 30 days. The incidence of access-site hematoma according to EASY scale. The incidence of radial artery occlusion at hospital discharge according to echo-doppler evaluation
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: At least two of the following additional criteria At least 70 yrs old Female gender Diabetes Creatinine clearance <60mL/min History of gastro-intestinal or other organ bleeding Baseline anemia Current treatment with glycoproteins IIb-IIIa inhibitors Exclusion Criteria: Intolerance or allergy to ASA, clopidogrel or ticlopidine precluding treatment for 12 months Concurrent participation in other investigational study Femoral sheath (artery)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Olivier F Bertrand, MD, PhD
Phone
418-656-8711
Email
olivier.bertrand@criucpq.ulaval.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Michele Jadin, MSc
Phone
418-656-8711
Ext
3007
Email
michele.jadin@criucpq.ulaval.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Olivier F Bertrand, MD, PhD
Organizational Affiliation
Fondation IUCPQ
Official's Role
Principal Investigator
Facility Information:
Facility Name
Quebec Heart-Lung Institute
City
Quebec
ZIP/Postal Code
G1V 4G5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michele Jadin, MSc
Phone
418-6568711
Ext
3007
Email
michele.jadin@crhl.ulaval.ca
First Name & Middle Initial & Last Name & Degree
Olivier F Bertrand, MD, PhD

12. IPD Sharing Statement

Learn more about this trial

EArly Discharge After Transradial Stenting of CoronarY Arteries in High-Risk Patients of Bleeding

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