Abstract:Objective: To evaluate impact of age, gender, race and BMI on NSAID efficacy in OA. Methods: Pfizer Clinical Trials Registry was searched for studies meeting the following criteria: randomized parallel-group design; Ն1 treatment group receiving celecoxib Ն200 mg daily; Ն1 placebo, NSAID, or rofecoxib comparator group; planned duration of Ն6 weeks; study completed and report finalized by October 31, 2004; 1 primary OA efficacy end point and pain visual analog scale (VAS) of 100 mm collected. In analyzing effica… Show more
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