Inpatient Versus Outpatient Foley Cervical Ripening Study

Status Completed

Clinical Trial Summary

To compare the efficacy and safety of cervical ripening with transcervical Foley catheter in inpatient vs outpatient setting

Clinical Trial Description

The aim of the current study is to compare the efficacy and safety of cervical ripening with transcervical Foley catheter in inpatient vs outpatient setting in a diverse, urban population within the United States. We hypothesize that there will be no differences in time-to-delivery, failed induction rates, cesarean section rates, or maternal/neonatal morbidity and that there will be no differences in total length of stay (LOS), hours of sleep, active labor duration, and perceived satisfaction between groups. ;

Study Design

Related Conditions & MeSH terms

Induced; Birth

Clinical Trial Details

NCT number	NCT03725397
Study type	Interventional
Source	Yale University
Contact
Status	Completed
Phase	N/A
Start date	January 8, 2019
Completion date	June 27, 2022

View Details

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