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Labor Induction With Misoprostol Versus Oxytocin in Women With Premature Rupture of Membranes

Premature Rupture of Membrane Clinical Trial

Official title:
Labor Induction With Misoprostol Versus Oxytocin in Women With Premature Rupture of Membranes

Clinical Trial Summary

This study compares the rate of vaginal delivery after induction of labor with misoprostol versus oxytocin in women with prelabor rupture of membranes. Participants will be randomized to receive either oral misoprotsol every four hours until going into labor, or intravenous oxytocin in increasing dose.

Clinical Trial Description

Misoprostol is a synthetic prostaglandin analogue commonly used for labor induction. It causes uterine contractions and ripening of the cervix. Oxytocin sold under the brand name Pitocin among others, is a medication made from the peptide oxytocin and is used to cause contraction of the uterus to start labor.

This randomized controlled trial will compare induction of labor in women with term premature rupture of the membranes and unripe cervix using misoprostol versus oxytocin. The primary outcome is the rate of vaginal delivery. Secondary outcomes will include cesarean section rate, time interval from induction of labor to delivery, neonatal morbidity, patient satisfaction and side effects, as well as chorioamnionitis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04143685
Study type Interventional
Source Bnai Zion Medical Center
Contact
Status Recruiting
Phase N/A
Start date December 1, 2019
Completion date October 1, 2021
View Details
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