Aspirin and Plavix Following Coronary Artery Bypass Grafting
Stopped early · Phase 4 · Has a placebo group
Conditions studied: Coronary Graft Patency
In brief
The design of the study will be randomized, double blind trial, which will examine the effects of addition of clopidogrel to current guideline recommended background therapy on lowering the incidence of graft stenosis after coronary artery bypass grafting compared to placebo.
Key facts
- Study ID
- NCT01158703
- Run by
- Ahmad Slim
- People needed
- 20
- Starts
- 2010-07-01
- Expected to finish
- 2014-12-01
- Last updated by the study team
- 2015-05-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Patients undergoing coronary artery bypass grafting, with or without cardiopulmonary bypass
- Age ≥ 18
You may not qualify if…
- Left ventricle ejection fraction <30%
- Emergency surgery
- Valve surgery
- Redo CABG
- Postoperative cardiogenic shock for more than 48 hours
- Postoperative bleeding or cardiac tamponade
- More than 24 hours postoperative intubation course
- Requirement of postoperative anticoagulation
- Serum creatinine >1.4
- Contraindication to use of postoperative coronary CT scan
- Allergy or contraindication to aspirin or clopidogrel
- Inability to provide informed consent
- Pregnant or breast feeding females
Where it is running
- Brooke Army Medical Center — San Antonio, Texas, United States
Full record on ClinicalTrials.gov
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