Clinical trial
Multicenter Study to Evaluate the Analgesic Efficacy of XP21L in Subjects With…
NCT00366444 · Xanodyne Pharmaceuticals, Industry · Completed
Key facts
| NCT number | NCT00366444 |
|---|---|
| Title | Multicenter Study to Evaluate the Analgesic Efficacy of XP21L in Subjects With Pain Following Bunionectomy Surgery |
| Official title | Multicenter Study to Evaluate the Analgesic Efficacy of XP21L in Subjects With Pain Following Bunionectomy Surgery |
| Lead sponsor | Xanodyne Pharmaceuticals, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Pain, Postoperative |
| Intervention type | Drug |
| Interventions | diclofenac potassium (XP21L), Placebo |
| Enrollment | 201 |
| Start date | Aug 1, 2006 |
| Primary completion | Oct 1, 2006 |
| First posted | Aug 21, 2006 |
| Last update posted | Apr 13, 2011 |
| Countries | United States |
At a glance
- 1–9 Study sites
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: