drugset / Trial / NCT00300196
ASP-II: Ancrod Stroke Program: Ancrod (Viprinex™) for the Treatment of Acute, Ischemic Stroke
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The primary purpose of this study is to determine whether a brief intravenous infusion of ancrod started within 6 hours of stroke onset improves functional outcome at 3 months.
Timeline
- Start
- 2006-03
- Primary completion
- 2008-12
- Completion
- 2008-12
Outcome
Outcome not reported
Stopped: “Futility”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ancrod | Unknown | 0.167 iu/kg | Intravenous |