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NCT00511992 · ClinicalTrials.gov registry record · Phase 2
Study of Bevacizumab Followed by Bevacizumab Consolidation for Ovarian Cancer
A Phase 2 study, sponsored by University of Oklahoma.
- Completed
- Registry status
- Phase 2
- Development phase
- 20
- Enrollment target
NCT00511992: Completed Phase 2 study, sponsored by University of Oklahoma.
NCT00511992 is a Phase 2 study that has completed, run by University of Oklahoma. The registered enrollment target is 20 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00511992, a Phase 2 study, has completed, sponsored by University of Oklahoma.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 20 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the tolerability of intraperitoneal cisplatin with intravenous paclitaxel and Avastin as defined by the proportion of patients able to complete 6 cycles of treatment.
Primary Outcome
Completion of cycle 6
Interventions
- DRUG Cisplatin
- DRUG Paclitaxel
- DRUG Avastin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2007-07 |
| Est. Completion | 2015-08-03 |
| Phase | Phase 2 |
What the finished NCT00511992 record still lists
NCT00511992 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower).
The record links to 0 conditions, and to 3 interventions - of which Cisplatin is the first listed.
NCT00511992 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00511992 about?
NCT00511992 is a clinical study titled "Study of Bevacizumab Followed by Bevacizumab Consolidation for Ovarian Cancer". The purpose of this study is to evaluate the tolerability of intraperitoneal cisplatin with intravenous paclitaxel and Avastin as defined by the proportion of patients able to complete 6 cycles of treatment.
What is the current status of trial NCT00511992?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2007-07. Estimated completion is 2015-08-03.
What interventions are being tested in trial NCT00511992?
The interventions under investigation include: Cisplatin (DRUG), Paclitaxel (DRUG), Avastin (DRUG).
Who is sponsoring clinical trial NCT00511992?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00511992's enrollment target sits among peer trials
20 1805th of 2000 higher than 107 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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