Trials / Completed
CompletedNCT00638807
Safety and Efficacy of Celecoxib Versus Placebo in the Treatment of Knee Osteoarthritis in Patients Who Were Unresponsive to Naproxen and Ibuprofen
A Double-Blind, Placebo Controlled Study of the Efficacy and Tolerability of Once Daily Celebrex (Celecoxib) vs. Placebo in the Treatment of Subjects With Osteoarthritis of the Knee Non-Responsive to Naproxen and Ibuprofen
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 388 (actual)
- Sponsor
- Pfizer's Upjohn has merged with Mylan to form Viatris Inc. · Industry
- Sex
- All
- Age
- 40 Years
- Healthy volunteers
- Not accepted
Summary
To compare the efficacy and safety of celecoxib versus placebo for the treatment of knee osteoarthritis (OA) in patients who were unresponsive to prescription strength naproxen and ibuprofen or who could not tolerate prescription strength naproxen and ibuprofen
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Celecoxib | 200 mg oral capsule once daily with morning meal for 6 weeks |
| OTHER | Placebo | Matched oral placebo for 6 weeks |
Timeline
- Start date
- 2003-12-01
- Completion
- 2004-07-01
- First posted
- 2008-03-19
- Last updated
- 2021-02-02
Locations
33 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00638807. Inclusion in this directory is not an endorsement.