Clinical Trials Directory

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

TypeNameDescription
DRUGCelecoxib200 mg oral capsule once daily for 12 weeks
DRUGCelecoxib200 mg oral capsule twice daily for 12 weeks
DRUGDiclofenac75 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.

Safety and Efficacy of Celecoxib Versus Diclofenac in the Treatment of Ankylosing Spondylitis (NCT00648141) · Clinical Trials Directory