drugset / Trial / NCT00618293
Haemate HS in Patients With Severe Bleeding Undergoing Valve Replacement Due to Aortic Stenosis
RandomizedParallel-groupTriple-blindTreatment
Summary
Evaluation of efficacy by determination of transfusion requirements and safety by determination of adverse events in administration of Von Willebrand factor concentrate F VIII (Haemate).
Timeline
- Start
- 2008-01
- Primary completion
- 2010-07
- Completion
- 2011-07
Outcome
Outcome not reported
Stopped: “No patient met the criteria for inclusion in the study.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Haemate HS | Protein / enzyme biologic | — | Intravenous |
Indications
No indication recorded.