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Reducing Time to Vaginal Delivery clinical trials

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NCT ID: NCT01127581 Completed - Cervical Ripening Clinical Trials

Efficacy & Safety Study Comparing Misoprostol Vaginal Insert (MVI) Versus Dinoprostone Vaginal Insert (DVI) for Reducing Time to Vaginal Delivery

EXPEDITE
Start date: September 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the Misoprostol Vaginal Insert (MVI) 200 microgram (mcg) can decrease the time to vaginal delivery compared to the Dinoprostone Vaginal Insert (DVI) 10 milligram (mg) in pregnant women requiring cervical ripening and induction of labor.