drugset / Trial / NCT00393731

A Randomized, Control Trial for Preinduction Cervical Ripening

NCT00393731

RandomizedSingle-groupSingle-blindTreatment

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.

Timeline

Start
2004-01
Primary completion
2007-08
Completion
2007-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Misoprostol Other / unclassified
Subject Oxytocin Peptide

Indications

No indication recorded.