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Clinical Trial Summary

The objective of this study is to compare reduced-dose prasugrel and standard dose clopidogrel in patients older than 74 years with ACS, including non-ST-elevation (NSTEACS) and ST-elevation (STEMI) patients, undergoing early PCI. The primary endpoint of the trial will be the one-year composite of (all-cause)death, myocardial infarction, stroke and re-hospitalization due to cardiovascular reasons or bleeding.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01777503
Study type Interventional
Source Arcispedale Santa Maria Nuova-IRCCS
Contact Stefano Savonitto, MD
Phone +39-0341-489490
Email s.savonitto@ospedale.lecco.it
Status Recruiting
Phase Phase 4
Start date November 2012
Completion date December 2017

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