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Plavix, Prasugrel and Drug Eluting Stents Pilot Trial — PPD  

Coronary Artery Disease Clinical Trial

Official title:
PPD Trial Pilot Study: Plavix, Prasugrel and Drug Eluting Stents

Clinical Trial 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).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01103843
Study type Interventional
Source St. Francis Hospital, New York
Contact Elizabeth S. Haag, RN, MPA CCRC
Phone 516 562-6790
Email elizabeth.haag@chsli.org
Status Unknown status
Phase N/A
Start date April 2010
Completion date May 2011
View Details
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