Cervical Ripening With Cook Catheter Plus Low Dose Oxytocin

Status Completed

Clinical Trial Summary

The purpose of this study is to compare if using a Cook Cervical Ripening Balloon in conjunction with low dose oxytocin is more effective at shortening labor induction times than the Cook Cervical Ripening Balloon alone. After obtaining consent, patients will be randomly divided into a Balloon with oxytocin or Balloon only group. The Balloon will be placed by either Resident or Attending Physicians and left in place for 12 hours (protocol) in both groups or until it falls out. After either 12 hours or the Balloon falls out, oxytocin will be used for the remainder of the induction per current hospital protocol. Time to delivery, mode of delivery, average number of hours Balloon remained in place, non-reassuring fetal heart tracings, adverse outcomes (ie fetal malpresentation, postpartum hemorrhage) will be recorded.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Cervical Ripening

Clinical Trial Details

NCT number	NCT02465164
Study type	Interventional
Source	Henry Ford Health System
Contact
Status	Completed
Phase	N/A
Start date	July 1, 2015
Completion date	July 30, 2016

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See also
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