drugset / Trial / NCT00374621

Trial of Cervical Ripening and Labor Induction Using Misoprostol With or Without Intravaginal Isosorbide Mononitrate

NCT00374621

Completed 156 enrolled Stanford University
RandomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the efficacy and safety of the addition of intravaginal isosorbide mononitrate to an established protocol of oral misoprostol for cervical ripening and labor induction.

Timeline

Start
2006-09
Primary completion
2007-12
Completion
2010-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Isosorbide Mononitrate Other / unclassified 40 mg Other
Comparator Misoprostol Other / unclassified 100 ug Oral

Indications