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Trial of Clopidogrel After Surgery for Coronary Artery Disease (CASCADE Trial) (CASCADE)

Primary Purpose

Atherosclerosis

Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Clopidogrel 75 mg daily
water pill daily
Sponsored by
Ottawa Heart Institute Research Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Atherosclerosis focused on measuring Saphenous vein, Intimal hyperplasia, Coronary artery bypass graft surgery, Antiplatelet therapy, Clopidogrel, Saphenous vein graft disease

Eligibility Criteria

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

Inclusion Criteria: Patients undergoing primary multi-vessel CABG with at least two saphenous vein grafts, with or without the use of cardiopulmonary bypass. Exclusion Criteria: Emergency surgery Valve surgery Redo CABG Left ventricle ejection fraction < 25% Serum creatinine > 130 µmol/L Preoperative use of clopidogrel (with the exception of the current admission) Preoperative use of warfarin; allergy to aspirin or clopidogrel. History of cerebrovascular accident History of severe liver disease Morbid obesity Current malignancy

Sites / Locations

  • University of Ottawa Heart Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

75mg Clopidogrel

Placebo

Arm Description

75mg clopidogrel. 162mg ASA is also given, but is a standard-of-care post operative to cardiac surgery.

Water pill. 162mg ASA is also given, but is a standard-of-care post operative to cardiac surgery.

Outcomes

Primary Outcome Measures

Vein Graft Intimal Area
IVUS imaging 12 months post-CABG, and the average intimal area in the proximal 40 mm of one vein graft per patient will be assessed

Secondary Outcome Measures

Vein Graft Angiographic Patency
Postoperative angiogram 12 months post-CABG
Incidence of Major Adverse Coronary Events Within One Year Following Surgery
Incidence of Major Bleeding Events Within One Year Following Surgery

Full Information

First Posted
September 26, 2005
Last Updated
March 30, 2021
Sponsor
Ottawa Heart Institute Research Corporation
Collaborators
Sanofi, Bristol-Myers Squibb
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1. Study Identification

Unique Protocol Identification Number
NCT00228423
Brief Title
Trial of Clopidogrel After Surgery for Coronary Artery Disease (CASCADE Trial)
Acronym
CASCADE
Official Title
Clopidogrel After Surgery for Coronary Artery Disease (CASCADE Trial): Does Clopidogrel Prevent Saphenous Vein Graft Disease After Coronary Bypass?
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
May 2006 (undefined)
Primary Completion Date
June 2009 (Actual)
Study Completion Date
July 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ottawa Heart Institute Research Corporation
Collaborators
Sanofi, Bristol-Myers Squibb

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine whether the combination of clopidogrel with aspirin prevents the development of blockages (atherosclerosis) in vein grafts one year after coronary artery bypass surgery (CABG) compared to aspirin alone.
Detailed Description
Saphenous vein graft disease remains a major limitation of coronary artery bypass graft surgery (CABG). The process of saphenous vein intimal hyperplasia is mediated by platelet aggregation and begins just days after surgical revascularization. Subsequently, areas of intimal hyperplasia in turn develop graft atherosclerotic disease and its sequelae. Clopidogrel improves outcomes in patients with atherosclerotic disease, and is effective at reducing intimal hyperplasia in animal models of thrombosis. Therefore, the goal of this study will be to evaluate the efficacy of clopidogrel and aspirin therapy versus aspirin alone in the prevention of saphenous vein graft intimal hyperplasia following one year after CABG. Patients undergoing multi-vessel CABG and in whom at least two saphenous vein grafts will be used are eligible for the study. Patients will be randomized to receive daily clopidogrel 75 mg or placebo, in addition to daily aspirin 162 mg, for the duration of one year starting as soon as postoperative bleeding has been ruled out on the day of surgery. At the end of one year, all patients will undergo coronary angiography and intravascular ultrasound assessment of one saphenous vein graft as selected by randomization. The study will be powered to test the hypothesis that clopidogrel and aspirin will reduce vein graft intimal hyperplasia by 20% compared to aspirin alone at one year following bypass surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atherosclerosis
Keywords
Saphenous vein, Intimal hyperplasia, Coronary artery bypass graft surgery, Antiplatelet therapy, Clopidogrel, Saphenous vein graft disease

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
113 (Actual)

8. Arms, Groups, and Interventions

Arm Title
75mg Clopidogrel
Arm Type
Active Comparator
Arm Description
75mg clopidogrel. 162mg ASA is also given, but is a standard-of-care post operative to cardiac surgery.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Water pill. 162mg ASA is also given, but is a standard-of-care post operative to cardiac surgery.
Intervention Type
Drug
Intervention Name(s)
Clopidogrel 75 mg daily
Intervention Description
Daily dose of 75 mg Clopidogrel
Intervention Type
Drug
Intervention Name(s)
water pill daily
Intervention Description
Daily dose of water pill (placebo)
Primary Outcome Measure Information:
Title
Vein Graft Intimal Area
Description
IVUS imaging 12 months post-CABG, and the average intimal area in the proximal 40 mm of one vein graft per patient will be assessed
Time Frame
One year following surgery
Secondary Outcome Measure Information:
Title
Vein Graft Angiographic Patency
Description
Postoperative angiogram 12 months post-CABG
Time Frame
One year following surgery
Title
Incidence of Major Adverse Coronary Events Within One Year Following Surgery
Time Frame
1 year
Title
Incidence of Major Bleeding Events Within One Year Following Surgery
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients undergoing primary multi-vessel CABG with at least two saphenous vein grafts, with or without the use of cardiopulmonary bypass. Exclusion Criteria: Emergency surgery Valve surgery Redo CABG Left ventricle ejection fraction < 25% Serum creatinine > 130 µmol/L Preoperative use of clopidogrel (with the exception of the current admission) Preoperative use of warfarin; allergy to aspirin or clopidogrel. History of cerebrovascular accident History of severe liver disease Morbid obesity Current malignancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marc Ruel, MD, MPH
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Alexander Kulik, MD
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Michel Le May, MD
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
George A Wells, PhD
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Thierry G Mesana, MD, PhD
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Study Director
Facility Information:
Facility Name
University of Ottawa Heart Institute
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1Y 4W7
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
8772748
Citation
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Results Reference
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PubMed Identifier
9521341
Citation
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Results Reference
background
PubMed Identifier
1531345
Citation
Jawien A, Bowen-Pope DF, Lindner V, Schwartz SM, Clowes AW. Platelet-derived growth factor promotes smooth muscle migration and intimal thickening in a rat model of balloon angioplasty. J Clin Invest. 1992 Feb;89(2):507-11. doi: 10.1172/JCI115613.
Results Reference
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PubMed Identifier
9759636
Citation
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Results Reference
background
PubMed Identifier
8343491
Citation
Herbert JM, Tissinier A, Defreyn G, Maffrand JP. Inhibitory effect of clopidogrel on platelet adhesion and intimal proliferation after arterial injury in rabbits. Arterioscler Thromb. 1993 Aug;13(8):1171-9. doi: 10.1161/01.atv.13.8.1171.
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PubMed Identifier
11958809
Citation
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PubMed Identifier
9832493
Citation
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PubMed Identifier
10859288
Citation
Cadroy Y, Bossavy JP, Thalamas C, Sagnard L, Sakariassen K, Boneu B. Early potent antithrombotic effect with combined aspirin and a loading dose of clopidogrel on experimental arterial thrombogenesis in humans. Circulation. 2000 Jun 20;101(24):2823-8. doi: 10.1161/01.cir.101.24.2823.
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PubMed Identifier
11157686
Citation
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PubMed Identifier
15313956
Citation
Fox KA, Mehta SR, Peters R, Zhao F, Lakkis N, Gersh BJ, Yusuf S; Clopidogrel in Unstable angina to prevent Recurrent ischemic Events Trial. Benefits and risks of the combination of clopidogrel and aspirin in patients undergoing surgical revascularization for non-ST-elevation acute coronary syndrome: the Clopidogrel in Unstable angina to prevent Recurrent ischemic Events (CURE) Trial. Circulation. 2004 Sep 7;110(10):1202-8. doi: 10.1161/01.CIR.0000140675.85342.1B. Epub 2004 Aug 16.
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PubMed Identifier
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Citation
Kulik A, Le May M, Wells GA, Mesana TG, Ruel M. The clopidogrel after surgery for coronary artery disease (CASCADE) randomized controlled trial: clopidogrel and aspirin versus aspirin alone after coronary bypass surgery [NCT00228423]. Curr Control Trials Cardiovasc Med. 2005 Oct 11;6(1):15. doi: 10.1186/1468-6708-6-15.
Results Reference
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PubMed Identifier
21135365
Citation
Kulik A, Le May MR, Voisine P, Tardif JC, Delarochelliere R, Naidoo S, Wells GA, Mesana TG, Ruel M. Aspirin plus clopidogrel versus aspirin alone after coronary artery bypass grafting: the clopidogrel after surgery for coronary artery disease (CASCADE) Trial. Circulation. 2010 Dec 21;122(25):2680-7. doi: 10.1161/CIRCULATIONAHA.110.978007. Epub 2010 Dec 6.
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PubMed Identifier
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Citation
Kulik A, Voisine P, Mathieu P, Masters RG, Mesana TG, Le May MR, Ruel M. Statin therapy and saphenous vein graft disease after coronary bypass surgery: analysis from the CASCADE randomized trial. Ann Thorac Surg. 2011 Oct;92(4):1284-90; discussion 1290-1. doi: 10.1016/j.athoracsur.2011.04.107.
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PubMed Identifier
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Citation
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Citation
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Citation
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Results Reference
derived
Links:
URL
http://www.ottawaheart.ca/
Description
University of Ottawa Heart Institute Website

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Trial of Clopidogrel After Surgery for Coronary Artery Disease (CASCADE Trial)

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