Status:
COMPLETED
Trial of Cervical Ripening and Labor Induction Using Misoprostol With or Without Intravaginal Isosorbide Mononitrate
Lead Sponsor:
Stanford University
Conditions:
Cervical Ripening
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief 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 ...
Eligibility Criteria
Inclusion
- :
- Pregnant women
- 18 years of age or greater
- Singleton pregnancy between 32-42 weeks gestation requiring labor induction
- Membranes must be intact
Exclusion
- Ruptured membranes
- Gestational age less than 32 weeks
- Non-reassuring fetal heart rate tracing
Key Trial Info
Start Date :
September 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2010
Estimated Enrollment :
156 Patients enrolled
Trial Details
Trial ID
NCT00374621
Start Date
September 1 2006
End Date
January 1 2010
Last Update
April 25 2017
Active Locations (1)
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1
Stanford University School of Medicine
Stanford, California, United States, 94305