Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02609607Phase 2Terminated
Phase 2, randomised, double-blind trial in constipation and fecal incontinence (FI) comparing Placebo Arm with Bisacodyl Arm (2 arms). Primary endpoint: Number of Participants With 30% Improvement From Baseline in Bowel Symptoms at 4 weeks. Started Jun 2016; 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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