Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT00671060Phase 3Completed
Phase 3, randomised, double-blind trial of misoprostol in intrauterine fetal demise (IUFD) (2 arms), sponsored by Gynuity Health Projects. Primary endpoint: Successful Expulsion of Fetus and Placenta Within 48 Hours. Started Oct 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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