drugset / Trial / NCT01736852

Evaluation of CRB in PROM Patients

NCT01736852

Completed 129 enrolled Cook Group Incorporated
RandomizedParallel-groupOpen-labelTreatment

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).

Timeline

Start
2012-11
Primary completion
2018-12-31
Completion
2018-12-31

Drugs

EvaluationDrugModalityDoseRoute
Background Oxytocin Peptide