Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT01733329Phase 4Completed
Phase 4, randomised, double-blind trial in postpartum hemorrhage (PPH) and uterine atony comparing Misoprostol with Placebo (2 arms). Primary endpoint: Need for Additional Uterotonic Medications at 24 hours. Started Feb 2008; 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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