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

Completed · Not applicable

Conditions studied: Cervical Ripening

In brief

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.

Key facts

Study ID

NCT00374621

Run by

Stanford University

People needed

156

Starts

2006-09-01

Expected to finish

2010-01-01

Last updated by the study team

2017-04-25

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may not qualify if…

• Ruptured membranes
• Gestational age less than 32 weeks
• Non-reassuring fetal heart rate tracing

Where it is running

• Stanford University School of Medicine — Stanford, California, United States

Full record on ClinicalTrials.gov

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