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A 4-week, Multicentre, Randomized, Double-blind, Double-dummy, Parallel Group Ambulatory Blood Pressure Monitoring Study to Investigate Whether Treatment With Lumiracoxib 100 mg Once Daily Results in an Improved 24-hour Blood Pressure Profile Compared to Ibuprofen 600 mg Three Times a Day in Osteoarthritis Patients With Controlled Hypertension

NCT00267176 Phase 4 COMPLETED

This study will investigate the effect on ambulatory blood pressure of lumiracoxib 100 mg once daily versus ibuprofen 600 mg three times a day in osteoarthritis patients with controlled hypertension.

Details

Lead sponsorNovartis Pharmaceuticals
PhasePhase 4
StatusCOMPLETED
Enrolment1020
Start date2005-11

Conditions

Interventions

Primary outcomes

Countries

United States, Germany