drugset / Trial / NCT03748147

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

NCT03748147

Unknown 300 enrolled University of Cincinnati
RandomizedSingle-groupTriple-blindTreatment

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.

Timeline

Start
2018-12-10
Primary completion
2020-06-01
Completion
2021-03-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Misoprostol Other / unclassified 25 ug Oral
Subject Misoprostol Other / unclassified 50 ug Oral