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Cervical Ripening in Obese Women: Efficacy of 25 mcg Versus 50 mcg of Misoprostol

Induction of Labor Affected Fetus / Newborn Clinical Trial

Official title:
Cervical Ripening in Obese Women: a Prospective, Randomized Trial Comparing Efficacy of 25 mcg Versus 50 mcg of Misoprostol

Clinical Trial Summary

This is a prospective clinical trial to determine if 50 mcg versus 25 mcg po every four hours of misoprostol has improved efficacy and similar safety in obese women undergoing cesarean section.

Clinical Trial Description

We will perform a prospective, randomized, double-blind clinical trial with parallel assignment.

Obese women (delivery BMI 30 or more) who agree to participation will be randomly designated to receive either 25 mcg po q 4 hour (control) misoprosol versus 50 mcg po q 4 hours. Our primary outcome will be the rate of successful induction. Secondary outcomes will include ability to achieve a Bishop score greater than 7, time to active labor, and safety data including rate of tachysystole, non-reassuring fetal status, NICU admission. ;

Study Design

Related Conditions & MeSH terms

  • Induction of Labor Affected Fetus / Newborn
Clinical Trial Details
NCT number NCT03748147
Study type Interventional
Source University of Cincinnati
Contact Carri R Warshak, M.D.
Phone 513-558-8448
Email eaglercr@ucmail.uc.edu
Status Not yet recruiting
Phase N/A
Start date December 10, 2018
Completion date March 1, 2021
View Details
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