Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04190173Phase 3Unknown
Phase 3, randomised, double-blind trial in paralytic ileus comparing Prucalopride with Placebo (2 arms). Primary endpoint: Change of maximum bowel diameter from baseline at 120 hours. Status: unknown.
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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