drugset / Trial / NCT01167023
Prasugrel Versus Placebo in Adult Sickle Cell Disease
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this trial is to assess the safety of Prasugrel in adult patients with sickle cell disease (SCD) by monitoring the rate and severity of hemorrhagic events requiring medical intervention compared to placebo for 30 days.
Timeline
- Start
- 2010-07
- Primary completion
- 2011-06
- Completion
- 2011-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Prasugrel | Small molecule | 5 mg | Oral |