NCT03138252

Study of the Effectiveness of Cervical Ripening Balloon With and Without Oxytocin

Randomized Controlled Trial: Cervical Ripening Balloon With and Without Oxytocin for Cervical Ripening in Multiparas

• Status: Completed
• Phase: Phase 3
• Study type: Interventional
• Enrollment: 180 (actual)
• Sponsor: University Hospitals Cleveland Medical Center · Academic / Other
• Sex: Female
• Age: 18 Years
• Healthy volunteers: Accepted

Summary

Study Purpose: The purpose of this study is to determine the optimal method for induction of labor in multiparous women who present with an unfavorable cervix. Hypothesis: Our hypothesis is that using oxytocin while the cervical ripening balloon is in place will result in more rapid labor courses, without increasing morbidity or increasing the need for operative delivery.

Conditions

• Cervical Ripening
• Induction of Labor
• Multiparity

Interventions

Type	Name	Description
DRUG	Oxytocin

Timeline

• Start date: 2014-11-01
• Primary completion: 2017-07-01
• Completion: 2017-07-01
• First posted: 2017-05-03
• Last updated: 2022-05-04
• Results posted: 2022-05-04

Locations

1 site across 1 country: United States