Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02254525Phase 3Terminated
Phase 3, randomised, double-blind trial in postoperative pain comparing Ibuprofen 800 mg with Placebo (2 arms). Primary endpoint: Efficacy of intravenous ibuprofen for the management of postoperative pain at 24 hours. Started May 2012; status: terminated.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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