Trials / Completed
CompletedNCT01642940
Τicagrelor Versus Prasugrel in Diabetic Patients: a Pharmacodynamic Study
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- University of Patras · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
This is a prospective, randomized, single-center, single blind, investigator initiated, two period study of crossover design. Diabetic patients with Acute Coronary Syndrome (ACS), treated with oral and/or parenteral hypoglycaemic therapy for at least 1 month and subjected to percutaneous coronary intervention (PCI), will be randomized after a baseline platelet reactivity (PR) assessment (24 hours post PCI) while under clopidogrel in a 1:1 ratio to either prasugrel 10mg or ticagrelor 180mg for 15 days followed by crossover directly to the alternate therapy for an additional 15 days without an intervening washout period.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Prasugrel | Prasugrel 10mg/day |
| DRUG | Ticagrelor | Ticagrelor 90mg twice a day |
Timeline
- Start date
- 2012-06-01
- Primary completion
- 2012-09-01
- Completion
- 2012-09-01
- First posted
- 2012-07-17
- Last updated
- 2013-01-23
Locations
1 site across 1 country: Greece
Source: ClinicalTrials.gov record NCT01642940. Inclusion in this directory is not an endorsement.