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Clopidogrel and Aspirin for Coronary Artery Disease (TARGET-CABG Trial)

N/A
Waitlist Available
Research Sponsored by LifeBridge Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up index hospitalization
Awards & highlights

TARGET-CABG Trial Summary

Purpose: In patients with coronary artery disease, aspirin and Plavix are used increasingly to prevent the formation of blood clots in the coronary arteries. These drugs exert their beneficial effects by irreversibly blocking platelets, the compounds found in blood responsible for clotting after an injury or during a heart attack. However, these effects also place patients at increased risk for bleeding after coronary artery bypass surgery. Therefore, it is currently recommended to withhold Plavix therapy for 5 days before undergoing surgery in order to reduce the incidence of bleeding. However, it has been repeatedly shown that Plavix exerts variable effects on different patients, which may be partially explained by poor absorption, drug-drug interaction, and by variations in deoxyribonucleic acid (DNA) which constitutes your genes. In addition, the time required for platelets to regain function after Plavix treatment has been shown to vary between patients. Therefore, by measuring platelet function, it may be possible to determine the optimal amount of time required to withhold Plavix before undergoing bypass surgery, which may improve rates of bleeding following the procedure. The purpose of this study is to classify patients into groups based on platelet function in order to define the ideal time period for delaying surgery. By analyzing the amount of time required for platelet recovery, it is expected that surgery-related bleeding will decrease without increasing the risk of blood clot formation. Eligibility: Approximately 200 patients requiring CABG will be enrolled at Sinai Hospital, which is the only site where this study is being conducted. To be eligible you must: Be able to provide written informed consent. Be between the ages of 18-85 and require CABG. Currently be on aspirin therapy (81-325mg).

Eligible Conditions
  • Coronary Artery Disease

TARGET-CABG Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~during the index hospitalization
This trial's timeline: 3 weeks for screening, Varies for treatment, and during the index hospitalization for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
The primary endpoint is chest tube drainage.
Secondary outcome measures
The secondary endpoint is transfusion requirements.

TARGET-CABG Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Clopidogrel and AspirinExperimental Treatment1 Intervention
Group II: Aspirin onlyActive Control1 Intervention
Continue aspirin until surgery

Find a Location

Who is running the clinical trial?

LifeBridge HealthLead Sponsor
28 Previous Clinical Trials
4,168 Total Patients Enrolled
8 Trials studying Coronary Artery Disease
2,567 Patients Enrolled for Coronary Artery Disease

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~12 spots leftby May 2025