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A Comparison of Oral Misoprostol and Vaginal Misoprostol for Cervical Ripening and Induction of Labor

Pregnancy Clinical Trial

Official title:
A Comparison of Oral Misoprostol and Vaginal Misoprostol for Cervical Ripening and Induction of Labor

Clinical Trial Summary

The purpose of this study is to study if misoprostol administered orally is at least as effective as misoprostol administered vaginally for cervical ripening and the induction of labor. The main purpose is to show that oral misoprostol administration is non-inferior to vaginal misoprostol administration with respect to the time interval from misoprostol administration to onset of active phase of labor. The study is a non-inferiority, prospective randomized controlled trial comparing oral misoprostol given as 25 mcg every 2 hours versus vaginal misoprostol given as 25 mcg every 4 hours.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

  • Labor; Forced or Induced, Affecting Fetus or Newborn
  • Pregnancy
Clinical Trial Details
NCT number NCT02777190
Study type Interventional
Source Milton S. Hershey Medical Center
Contact
Status Terminated
Phase Phase 4
Start date November 1, 2017
Completion date April 23, 2019
View Details
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