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NCT00293631 · ClinicalTrials.gov registry record · Phase 2
Study of Lornoxicam or Ketorolac or Placebo for Post-Operative Pain After Bunionectomy
A Phase 2 study, sponsored by POZEN.
- Completed
- Registry status
- Phase 2
- Development phase
- 100
- Enrollment target
NCT00293631: Completed Phase 2 study, sponsored by POZEN.
NCT00293631 is a Phase 2 study that has completed, run by POZEN. The registered enrollment target is 100 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (25% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00293631, a Phase 2 study, has completed, sponsored by POZEN.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 100 participants
- Enrollment target
Study Summary
To determine whether a single dose of intravenous lornoxicam is superior to intravenous placebo for management of post-operative pain in patients who have surgical removal of a bunion on the lower extremity. One-fourth of patients in this study will receive a single dose of intravenous ketorolac for management of pain and one-fourth of patients in this study will receive a single dose of an intravenous placebo.
Interventions
- DRUG Placebo
- DRUG Lornoxicam 8 mg
- DRUG Lornoxicam 16 mg
- DRUG Ketorolac 30 mg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2005-11 |
| Est. Completion | 2006-03 |
| Phase | Phase 2 |
What the finished NCT00293631 record still lists
NCT00293631 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (25% lower).
The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.
NCT00293631 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00293631 about?
NCT00293631 is a clinical study titled "Study of Lornoxicam or Ketorolac or Placebo for Post-Operative Pain After Bunionectomy". To determine whether a single dose of intravenous lornoxicam is superior to intravenous placebo for management of post-operative pain in patients who have surgical removal of a bunion on the lower extremity. One-fourth of patients in this study will receive a single dose of intravenous ketorolac for...
What is the current status of trial NCT00293631?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 100 participants. The study started on 2005-11. Estimated completion is 2006-03.
What interventions are being tested in trial NCT00293631?
The interventions under investigation include: Placebo (DRUG), Lornoxicam 8 mg (DRUG), Lornoxicam 16 mg (DRUG), Ketorolac 30 mg (DRUG).
Who is sponsoring clinical trial NCT00293631?
This trial is sponsored by POZEN, which has 24 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00293631's enrollment target sits among peer trials
100 672nd of 2000 higher than 1,263 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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