Trials / Completed
CompletedNCT00648141
Safety and Efficacy of Celecoxib Versus Diclofenac in the Treatment of Ankylosing Spondylitis
A 12-Week Symptomatic Effect Evaluation to Compare Celecoxib 200 mg QD, Celecoxib 200 mg BID and Diclofenac 75 mg SR BID in Patients With Ankylosing Spondylitis
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 458 (actual)
- Sponsor
- Pfizer · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
To compare the safety and efficacy of once-daily and twice-daily celecoxib versus diclofenac for the treatment of ankylosing spondylitis
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Celecoxib | 200 mg oral capsule once daily for 12 weeks |
| DRUG | Celecoxib | 200 mg oral capsule twice daily for 12 weeks |
| DRUG | Diclofenac | 75 mg oral capsule twice daily for 12 weeks |
Timeline
- Start date
- 2003-01-01
- Completion
- 2005-01-01
- First posted
- 2008-04-01
- Last updated
- 2008-04-10
Locations
47 sites across 1 country: Germany
Source: ClinicalTrials.gov record NCT00648141. Inclusion in this directory is not an endorsement.