This protocol is designed to evaluate the effect of antiplatelets (Tirafiban and Prasugrel)
on the incidence of early and intermediate graft patency after CABG.
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Locations near you
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Full eligibility criteria for NCT01598337
Ages eligible for Study
18 Years to 75 Years
Genders eligible for Study
Accepts Healthy Volunteers
All comer study where all patients undergoing coronary bypass surgery (CABG) will be randomized to one of the four treatment groups
Acute myocardial infarction (AMI) or cardiogenic shock
Contraindication to antiplatelets or aggrastat.
Active bleeding or high risk of bleeding.
History of hemorrhagic stroke any time.
Recent history of embolic stroke or transient ischemic attack (TIA) less than 3 months.
Active peptic ulcer disease (PUD).
Heparin-induced thrombocytopenia (HIT) syndrome.
Thrombocytopenia (platelet count <100,000/mm3), disorders of platelet function
All locations for NCT01598337
Saudi Arabia (1)
Prince Sultan Cardiac Center
Riyadh, Saudi Arabia
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View full eligibility
Tris trial is registered with FDA with number: NCT01598337. The sponsor of the trial is Prince Sultan Cardiac Center, Adult Cardiology Department. and it is looking for 200 volunteers for the current phase.
Official trial title: The Effect Of Antiplatelets Therapy, Tirafiban, Prasugrel, And Aspirin On Saphenous Vein Coronary Artery Bypass Graft Patency
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