A Randomized, Control Trial for Preinduction Cervical Ripening
Status:
Completed
Trial end date:
2007-08-01
Target enrollment:
Participant gender:
Summary
The goal of this study is to compare the vaginal delivery rates in women undergoing induction
of labor with an unripe cervix between oxytocin induction alone and preinduction cervical
ripening with prostaglandin El (misoprostol). Secondary goals are to measure and compare the
time intervals to delivery between the two methods.
Phase:
Phase 2
Details
Lead Sponsor:
The University of Texas Health Science Center, Houston