Clinical trial
Study of Lornoxicam or Ketorolac or Placebo for Post-Operative Pain After…
NCT00293631 · POZEN, Industry · Completed
Key facts
| NCT number | NCT00293631 |
|---|---|
| Title | Study of Lornoxicam or Ketorolac or Placebo for Post-Operative Pain After Bunionectomy |
| Official title | A Randomized, Parallel-Group, Double-Blind, Single-Dose Study Evaluating the Efficacy and Safety of Intravenous Lornoxicam (8 mg and 16 mg) Compared to Intravenous Placebo and Ketorolac 30 mg in Management of Acute Postoperative Pain Following Orthopedic Surgery (Bunionectomy). |
| Lead sponsor | POZEN, Industry |
| Status | Completed |
| Phase | Phase 2 |
| Study type | Interventional |
| Conditions | Bunionectomy, Orthopedic Surgery |
| Intervention type | Drug |
| Interventions | Lornoxicam 8 mg, Lornoxicam 16 mg, Ketorolac 30 mg, Placebo |
| Enrollment | 100 |
| Start date | Nov 1, 2005 |
| Primary completion | Mar 1, 2006 |
| Completion | Mar 1, 2006 |
| First posted | Feb 17, 2006 |
| Last update posted | Dec 3, 2012 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No 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: