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

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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).


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
(713) 500-4472
University of Texas Health Science Center at Houston The University of Texas Health Science Center...
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Houston, TX
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4202 E Fowler Ave
Tampa, Florida 33620
(813) 974-2011
University of South Florida The University of South Florida is a high-impact, global research university...
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Tampa, FL
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Louisville, KY
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Tucson, Arizona 85712
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Tucson, AZ
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