Clinical Trials Directory

Trials / Completed

CompletedNCT01835353

High (100mg) Versus Standard (60mg) Loading Dose of Prasugrel in Patients With ST-elevation Myocardial Infarction (STEMI), Undergoing Primary Percutaneous Coronary Intervention (PCI)

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
82 (actual)
Sponsor
University of Patras · Academic / Other
Sex
All
Age
18 Years – 74 Years
Healthy volunteers
Not accepted

Summary

This is a prospective, multi-center, non-randomized, controlled study in 2 sequential groups of P2Y12 inhibitor-naive consecutive STEMI patients undergoing primary PCI. Following aspirin 325 mg LD, patients will receive 60 mg or 100 mg of prasugrel, respectively. Platelet reactivity (PR)will be assessed at Hour 0 (before prasugrel's administration immediately prior to PCI) and at Hours 0.5, 1, 2, 4 thereafter. Platelet function testing (in PRU) will be performed with the VerifyNow (Accumetrics Inc., San Diego, CA, USA) P2Y12 function assay.

Conditions

Interventions

TypeNameDescription
DRUGPrasugrel 100mg loading dose
DRUGPrasugrel 60mg loading dosePrasugrel 60mg loading dose

Timeline

Start date
2012-06-01
Primary completion
2013-07-01
Completion
2013-07-01
First posted
2013-04-18
Last updated
2013-09-23

Locations

1 site across 1 country: Greece

Source: ClinicalTrials.gov record NCT01835353. Inclusion in this directory is not an endorsement.