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NCT00656578 · ClinicalTrials.gov registry record · Phase 3
Efficacy and Safety Study of 4975 to Manage Pain of Bunionectomy
A Phase 3 study, sponsored by Anesiva.
- Completed
- Registry status
- Phase 3
- Development phase
- 300
- Enrollment target
NCT00656578: Completed Phase 3 study, sponsored by Anesiva.
NCT00656578 is a Phase 3 study that has completed, run by Anesiva. The registered enrollment target is 300 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (61% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00656578, a Phase 3 study, has completed, sponsored by Anesiva.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 300 participants
- Enrollment target
Study Summary
The primary purpose of this study is to compare the analgesic efficacy of a single intraoperative administration of 4975 vs. Placebo in the management of acute postoperative pain in patients undergoing bunionectomy. Secondary objective of this study is to evaluate the safety and tolerability of a single intraoperative administration of 4975.
Interventions
- DRUG Placebo
- DRUG 4975
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 300 participants |
| Start Date | 2008-03 |
| Est. Completion | 2008-09 |
| Phase | Phase 3 |
What the finished NCT00656578 record still lists
NCT00656578 is an interventional study that assigns participants to a tested intervention. The registered 300 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (61% lower).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT00656578 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00656578 about?
NCT00656578 is a clinical study titled "Efficacy and Safety Study of 4975 to Manage Pain of Bunionectomy". The primary purpose of this study is to compare the analgesic efficacy of a single intraoperative administration of 4975 vs. Placebo in the management of acute postoperative pain in patients undergoing bunionectomy. Secondary objective of this study is to evaluate the safety and tolerability of a s...
What is the current status of trial NCT00656578?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 300 participants. The study started on 2008-03. Estimated completion is 2008-09.
What interventions are being tested in trial NCT00656578?
The interventions under investigation include: Placebo (DRUG), 4975 (DRUG).
Who is sponsoring clinical trial NCT00656578?
This trial is sponsored by Anesiva, which has 7 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00656578's enrollment target sits among peer trials
300 1122nd of 2000 higher than 840 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 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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