Evaluation of CRB in PROM Patients
| Status: | Completed |
|---|---|
| Conditions: | Women's Studies |
| Therapuetic Areas: | Reproductive |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 1/20/2019 |
| Start Date: | November 2012 |
| End Date: | December 31, 2018 |
Randomized Study to Compare the Cook Cervical Ripening Balloon Plus Pitocin to Pitocin Alone in PROM Patients
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).
Balloon (CRB) for the induction of labor in term and near-term patients with premature
rupture of membranes (PROM).
Inclusion Criteria:
- PROM not in labor
Exclusion Criteria:
- Contraindication to vaginal delivery
- Contraindication to labor induction
- Abnormal fetal heart-rate patterns
- Maternal heart disease
- Severe maternal hypertension
- Pelvic structural abnormality
We found this trial at
4
sites
7000 Fannin St
Houston, Texas 77030
Houston, Texas 77030
(713) 500-4472
University of Texas Health Science Center at Houston The University of Texas Health Science Center...
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University of South Florida The University of South Florida is a high-impact, global research university...
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