Trial of Cervical Ripening and Labor Induction Using Misoprostol With or Without Intravaginal Isosorbide Mononitrate
Trial ID or NCT#
NCT00374621
Status
NOT RECRUITING
Purpose
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.
Official Title
Randomized Clinical Trial of Cervical Ripening and Labor Induction Using Stepwise Oral Misoprostol With or Without Intravaginal Isosorbide Mononitrate
Eligibility Criteria
Ages Eligible for Study: Older than 18 Years
Sexes Eligible for Study: Female
Accepts Healthy Volunteers: No
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
Investigator(s)
Yasser El-Sayed, Professor
Obstetrician and Gynecologist (OB-GYN)
Charles B. and Ann L. Johnson Professor in the School of Medicine and Professor, by courtesy, of Pediatrics (Neonatology) and of Surgery
Contact us to find out if this trial is right for you.
Contact
Yasser El-Sayed
6507233198
View on ClinicalTrials.gov
