drugset / Trial / NCT00170781

Efficacy and Safety of Lumiracoxib 400 mg Once Daily in Acute Flares of Gout

NCT00170781

Phase 4 Completed 234 enrolled Novartis
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is designed to develop our understanding of the efficacy and safety of using lumiracoxib in the treatment of patients with acute gout. This is a multi-center, double-blind, randomized, parallel group study comparing a single daily dose of 400 mg lumiracoxib with the established dose of indomethacin 50 mg taken three times a day in terms of efficacy

Timeline

Start
2005-06
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Lumiracoxib Small molecule 400 mg

Indications