Evaluation of CRB in PROM Patients

Premature Rupture of Fetal Membranes Clinical Trial

Official title:
Randomized Study to Compare the Cook Cervical Ripening Balloon (CRB) Plus Pitocin to Pitocin Alone in Premature Rupture of Membranes (PROM) Patients

Status Completed

Clinical Trial Summary

The CRB study is designed to study the safety and effectiveness of the Cook Cervical Ripening Balloon (CRB) for the induction of labor in term and near-term patients with premature rupture of membranes (PROM).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Fetal Membranes, Premature Rupture
Premature Birth
Premature Rupture of Fetal Membranes
Rupture

Clinical Trial Details

NCT number	NCT01736852
Study type	Interventional
Source	Cook Group Incorporated
Contact
Status	Completed
Phase	N/A
Start date	November 2012
Completion date	December 31, 2018

View Details

See also
Status	Clinical Trial	Phase
Not yet recruiting	`NCT02801227` - Oxytocin vs. Prostaglandin for Induction of Labor in Primiparas With Prelabor Rupture of Membrane and Low Bishop	Phase 4
Completed	`NCT00940043` - Monitoring of the Inflammatory Response of Patients With Premature Rupture of Membranes With Bedside Tests	N/A
Not yet recruiting	`NCT03025581` - Does Nipple Stimulation Shorten Time to Vaginal Birth in Women With Term PROM?	N/A
Recruiting	`NCT05568745` - Balloon + Oxytocin Versus Oral Misoprostol to Induce Labor in Case of PROM (RUBAPRO2)	Phase 4
Recruiting	`NCT03108404` - Predictive Score for Neonatal Mortality for Women With Premature Rupture of Membranes Between 22 and 28 Weeks of Gestation	N/A