Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT00141895Phase 3Terminated
Phase 3, randomised, open-label trial of misoprostol in intrauterine fetal demise (IUFD) (2 arms), sponsored by American University of Beirut Medical Center. Primary endpoint: Induction time at 48 hours. Started Sep 2004; 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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