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Aspirin Non-responsiveness and Clopidogrel Endpoint Trial. (ASCET)

Primary Purpose

Coronary Heart Disease, Angina Pectoris, Atherosclerosis

Status
Completed
Phase
Phase 4
Locations
Norway
Study Type
Interventional
Intervention
aspirin
clopidogrel
Sponsored by
Ullevaal University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Heart Disease focused on measuring antiplatelet therapy, aspirin non-responders, aspirin resistance, clopidogrel, coronary heart disease, stable angina pectoris

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Stable, symptomatic coronary heart disease, verified by coronary angiography, being treated with angioplasty/stent implantation (PCI) or not. Exclusion Criteria: Indication for warfarin treatment. Indication for or contraindication to the study drugs. Pregnancy or breast-feeding. Malignancy that may interfere with life expectancy. Psychiatric disease, mental retardation, dementia, drug abuse, alcoholism or conditions that can severely reduce compliance.

Sites / Locations

  • Ullevaal University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1, aspirin

2, clopidogrel

Arm Description

Aspirin 160 mg

Clopidogrel 75 mg

Outcomes

Primary Outcome Measures

Mortality
Myocardial infarction
Unstable angina with ECG changes or raised levels of cardiac markers not to be classified as a myocardial infarction

Secondary Outcome Measures

Instent restenosis and/or thrombosis detected by coronary angiography.

Full Information

First Posted
September 13, 2005
Last Updated
March 22, 2011
Sponsor
Ullevaal University Hospital
Collaborators
The Norwegian Council for Cardiovascular Diseases., Ada and Hagbart Waages Humanitarian and Charity Foundation, Alf and Aagot Helgesens Research Foundation.
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1. Study Identification

Unique Protocol Identification Number
NCT00222261
Brief Title
Aspirin Non-responsiveness and Clopidogrel Endpoint Trial.
Acronym
ASCET
Official Title
Aspirin Non-responsiveness and Clopidogrel Endpoint Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2011
Overall Recruitment Status
Completed
Study Start Date
April 2003 (undefined)
Primary Completion Date
July 2010 (Actual)
Study Completion Date
July 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Ullevaal University Hospital
Collaborators
The Norwegian Council for Cardiovascular Diseases., Ada and Hagbart Waages Humanitarian and Charity Foundation, Alf and Aagot Helgesens Research Foundation.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In the ASCET study, 1000 patients with documented coronary heart disease will be randomized to either continued treatment with aspirin 160 mg/d or change to clopidogrel 75mg/d. Clinical endpoints will be recorded for at least 2 years and related to the initial aspirin response, assessed by the PFA-100® method, to investigate whether aspirin non-responders have higher composite event rate than responders or whether Clopidogrel treatment in patients non-responsive to aspirin will reduce their risk of future clinical events. The clinical events are the composite of unstable angina, myocardial infarction, stroke or death.
Detailed Description
Background: Aspirin is widely used as an antiplatelet drug in patients with coronary heart disease. Despite documented clinical benefit, many patients on aspirin still experience severe cardiovascular events. Several laboratory reports have shown lack of platelet inhibition in 5-40% of aspirin-treated patients, and the term aspirin resistance has been introduced. The clinical relevance of these laboratory findings is, however, still unknown. New antiplatelet drugs have been developed, and the adenosin diphosphate (ADP) receptor inhibitor clopidogrel has at least the same efficacy as aspirin with an acceptable safety profile. Laboratory methods for determination of platelet reactivity and treatment efficacy have been complicated and time consuming. New methodologies, like the PFA-100® system, have made such analyses more suitable for clinical use. Design: In the ASCET study, 1000 patients with documented coronary heart disease will be randomized to either continued treatment with aspirin 160 mg/d or change to clopidogrel 75mg/d after initial determination of their platelet reactivity while on aspirin treatment. Clinical endpoints will be recorded for at least 2 years and related to the initial aspirin response. Scand Cardiovasc J. 2004 Dec;38(6):353-6.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Heart Disease, Angina Pectoris, Atherosclerosis
Keywords
antiplatelet therapy, aspirin non-responders, aspirin resistance, clopidogrel, coronary heart disease, stable angina pectoris

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1001 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1, aspirin
Arm Type
Active Comparator
Arm Description
Aspirin 160 mg
Arm Title
2, clopidogrel
Arm Type
Active Comparator
Arm Description
Clopidogrel 75 mg
Intervention Type
Drug
Intervention Name(s)
aspirin
Intervention Description
Aspirin 160 mg once daily for two years
Intervention Type
Drug
Intervention Name(s)
clopidogrel
Intervention Description
clopidogrel 75 mg once daily for two years
Primary Outcome Measure Information:
Title
Mortality
Time Frame
2 years
Title
Myocardial infarction
Time Frame
2 years
Title
Unstable angina with ECG changes or raised levels of cardiac markers not to be classified as a myocardial infarction
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Instent restenosis and/or thrombosis detected by coronary angiography.
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Stable, symptomatic coronary heart disease, verified by coronary angiography, being treated with angioplasty/stent implantation (PCI) or not. Exclusion Criteria: Indication for warfarin treatment. Indication for or contraindication to the study drugs. Pregnancy or breast-feeding. Malignancy that may interfere with life expectancy. Psychiatric disease, mental retardation, dementia, drug abuse, alcoholism or conditions that can severely reduce compliance.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alf-Aage R. Pettersen, M.D.
Organizational Affiliation
Dept. of Cardiology, Ullevaal University Hospital, Oslo
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Harald Arnesen, M.D. Ph.D.
Organizational Affiliation
Center for Clinical Cardiovascular Research, Ullevaal University Hospital, Oslo
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ingebjorg Seljeflot, Ph.D.
Organizational Affiliation
Center for Clinical Cardiovascular Research, Ullevaal University Hospital, Oslo
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Michael Abdelnoor, Ph.D.
Organizational Affiliation
Center for Clinical Cardiovascular Research, Ullevaal University Hospital, Oslo
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Arne Westheim, M.D. Ph.D
Organizational Affiliation
Dept. of Cardiology, Ullevaal University Hospital, Oslo
Official's Role
Study Director
Facility Information:
Facility Name
Ullevaal University Hospital
City
Oslo
ZIP/Postal Code
0407
Country
Norway

12. IPD Sharing Statement

Citations:
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Citation
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Citation
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PubMed Identifier
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Citation
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Citation
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Aspirin Non-responsiveness and Clopidogrel Endpoint Trial.

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