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Vaginal Misoprostol With Intracervical Foley Catheter in Induction of Labor

Induction of Labor Affected Fetus / Newborn Clinical Trial

Official title:
Vaginal Misoprostol With Intracervical Foley Catheter Versus Vaginal Misoprostol Alone in Induction of Labor at Term Pregnancy

Clinical Trial Summary

The aim of present study is to compare the safety and efficacy of vaginal misoprostol versus the combination of vaginal misoprostol and intracervical Foley catheter in induction of labor at term pregnancy.

Clinical Trial Description

Cervical status is a good predictor of the likelihood of vaginal delivery when labor is induced. Any induction method is likely to be effective in a woman with a favorable cervix, whereas no method is highly successful when performed in a woman with a cervix that is unfavorable. The use of a balloon catheter as induction method was first described in 1862 by Trainer. The goal of the catheter was to ripen the cervix through direct mechanical dilatation of the cervical canal and indirectly by increasing endogenous prostaglandin secretion. Alternatively, Prostaglandins are one of the key players in cervical ripening by a number of different mechanisms. The aim of present study is to compare the safety and efficacy of vaginal misoprostol versus the combination of vaginal misoprostol and intracervical Foley catheter in induction of labor at term pregnancy. ;

Study Design

Related Conditions & MeSH terms

  • Induction of Labor Affected Fetus / Newborn
Clinical Trial Details
NCT number NCT03682718
Study type Interventional
Source Ain Shams University
Contact
Status Completed
Phase Phase 4
Start date October 1, 2018
Completion date February 1, 2019
View Details
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