Study design & results
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Trial intelligence / Profile preview
NCT02924480Completed
Randomised, double-blind trial in postoperative pain and postoperative ileus (POI) comparing Lidocaine Study Group with Placebo Study Group (2 arms). Primary endpoints: Reduced pain post-operatively using verbal analog score at 108 hours and Time until Ileus resolution at 108 hours. Started Oct 2016; status: completed.
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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