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NCT00168090 · ClinicalTrials.gov registry record · Phase 4
Study of Safety and Efficacy of Antihemophilic Factor/Von Willebrand Factor Complex in Surgical Subjects With Von Willebrand Disease (vWD)
A Phase 4 study, sponsored by CSL Behring.
- Completed
- Registry status
- Phase 4
- Development phase
- 30
- Enrollment target
NCT00168090: Completed Phase 4 study, sponsored by CSL Behring.
NCT00168090 is a Phase 4 study that has completed, run by CSL Behring. The registered enrollment target is 30 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00168090, a Phase 4 study, has completed, sponsored by CSL Behring.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 30 participants
- Enrollment target
Study Summary
The purpose of this study is to test the safety and effectiveness of Humate-P® to prevent bleeding in patients with von Willebrand Disease who are undergoing surgery.
Interventions
- DRUG Blood coagulation Factor VIII and vWF, human
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2001-10 |
| Est. Completion | 2006-05 |
| Phase | Phase 4 |
What the finished NCT00168090 record still lists
NCT00168090 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (94% lower).
The record links to 0 conditions, and to 1 intervention - of which Blood coagulation Factor VIII and vWF, human is the first listed.
NCT00168090 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00168090 about?
NCT00168090 is a clinical study titled "Study of Safety and Efficacy of Antihemophilic Factor/Von Willebrand Factor Complex in Surgical Subjects With Von Willebrand Disease (vWD)". The purpose of this study is to test the safety and effectiveness of Humate-P® to prevent bleeding in patients with von Willebrand Disease who are undergoing surgery.
What is the current status of trial NCT00168090?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 30 participants. The study started on 2001-10. Estimated completion is 2006-05.
What interventions are being tested in trial NCT00168090?
The interventions under investigation include: Blood coagulation Factor VIII and vWF, human (DRUG).
Who is sponsoring clinical trial NCT00168090?
This trial is sponsored by CSL Behring, which has 71 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00168090's enrollment target sits among peer trials
30 1552nd of 2000 higher than 367 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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