A Study to Evaluate the Efficacy and Safety of Celecoxib Suspension Compared to Naproxen Suspension in Patients With JRA
- Registration Number
- NCT00652925
- Lead Sponsor
- Pfizer
- Brief Summary
- To study Celebrex versus naproxen to see if it decreases symptoms of juvenile arthritis such as pain and swelling. 
- Detailed Description
- Not available 
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 225
Inclusion Criteria
2-18 years old with active JRA
Exclusion Criteria
other experimental meds, recent changes in arthritis meds
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
- Group - Intervention - Description - Low Dose - Celecoxib - - - Naproxen - Naproxen - Control comparator, 15 mg/kg/dy target dose - High Dose - Celecoxib - - 
- Primary Outcome Measures
- Name - Time - Method - ACR Pediatric 30 - 12 weeks 
- Secondary Outcome Measures
- Name - Time - Method - Peds QOL - 12 weeks - composites of acr 30 - 12 weeks 
Trial Locations
- Locations (1)
- Pfizer Investigational Site 🇸🇪- Stockholm, Sweden Pfizer Investigational Site🇸🇪Stockholm, Sweden
