drugset / Trial / NCT00886860

The Comparison of Efficacy for Cervical Ripening in Labor Induction Between Titrated and Conventional Oral Misoprostol

NCT00886860

Phase 4 Completed 64 enrolled Mahidol University
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to compare the efficacy for cervical ripening in labor induction between titrated and conventional oral misoprostol

Timeline

Start
2009-05
Primary completion
2009-12
Completion
2010-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Misoprostol Other / unclassified 40 ug Oral
Subject Misoprostol Other / unclassified 50 ug Oral

Indications