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
| Type | Name | Description |
|---|---|---|
| DRUG | Prasugrel 100mg loading dose | |
| DRUG | Prasugrel 60mg loading dose | Prasugrel 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.