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Misoprostol With Mechanical Dilation Versus Oxytocin With Mechanical Dilation for High-risk Pregnancy Inductions — MODE  

Cesarean Section Clinical Trial

Official title:
Misoprostol With Mechanical Dilation Versus Oxytocin With Mechanical Dilation for High-risk Pregnancy Inductions: A Randomized Control Trial

Clinical Trial Summary

The purpose of this study is to specifically investigate whether oxytocin and mechanical dilation decreases the rate of cesarean section compared to misoprostol and mechanical dilation for pregnancies at risk of fetal compromise

Clinical Trial Description

This is a single center randomized control trial of two arms. Singleton, cephalic, high risk pregnancies will be randomized to either oxytocin with mechanical dilation versus misoprostol with mechanical dilation. In group A, receiving misoprostol with mechanical dilation, will serve as the control group. Group B, oxytocin with mechanical dilation, will serve as the experimental group. The expected duration of participation begins at induction of labor and concludes at time of delivery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04492072
Study type Interventional
Source Thomas Jefferson University
Contact
Status Completed
Phase N/A
Start date August 17, 2020
Completion date May 26, 2022
View Details
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