drugset / Trial / NCT01103843

Plavix, Prasugrel and Drug Eluting Stents Pilot Trial

NCT01103843

Unknown 1000 enrolled St. Francis Hospital, New York
RandomizedCrossoverOpen-labelTreatment

Summary

* The purpose of this study is to determine the level of inhibition of platelet activation of an approved thienopyridine(clopidogrel or prasugrel) and aspirin regimen in the setting of drug eluting coronary stent implantation. * In subjects with high residual levels of platelet reactivity after receiving either a maintenance or loading dose of either clopidogrel or prasugrel, a cross over of thienopyridine treatment to the alternate medication will occur. * The study tests the hypothesis that adequate platelet inhibition will occur in subjects who have high levels of platelet reactivity and are subsequently switched from clopidogrel to prasugrel(loading or maintenance dose) without increased episodes of bleeding or MACE events at discharge and 30 days post Percutaneous Coronary Intervention (PCI).

Timeline

Start
2010-04
Primary completion
2011-04
Completion
2011-05

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Clopidogrel Small molecule 75 mg
Comparator Clopidogrel Small molecule 600 mg
Comparator Prasugrel Small molecule 10 mg
Comparator Prasugrel Small molecule 60 mg