Trial Search Results

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

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.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Stanford University

Stanford Investigator(s):

Intervention(s):

  • Drug: Misoprostol with or without isosorbide mononitrate

Phase:

N/A

Eligibility


Inclusion Criteria::

   - Pregnant women

   - 18 years of age or greater

   - Singleton pregnancy between 32-42 weeks gestation requiring labor induction

   - Membranes must be intact

Exclusion Criteria:

   - Ruptured membranes

   - Gestational age less than 32 weeks

   - Non-reassuring fetal heart rate tracing

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

Female

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Yasser El-Sayed
6507233198
Not Recruiting