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Cervical Ripening as an Outpatient Method Using the Foley (COMFORT) — COMFORT  

Induction of Labor Affected Fetus / Newborn Clinical Trial

Official title:
Cervical Ripening as an Outpatient Method Using the Foley: a Randomized Trial

Clinical Trial Summary

A multicenter pragmatic randomized trial of nulliparous women undergoing a term (≥37 weeks) induction of labor wherein the provider intends to use a Foley catheter for cervical ripening. The investigators will be comparing outpatient cervical ripening with a Foley catheter to routine inpatient cervical ripening (Foley +/- other method). With this trial, the investigators aim to test our central hypothesis that outpatient Foley will decrease the primary Cesarean Delivery (CD) rate and risk of maternal/neonatal morbidity compared with inpatient cervical ripening.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

  • Induction of Labor Affected Fetus / Newborn
Clinical Trial Details
NCT number NCT05759988
Study type Interventional
Source University of Pennsylvania
Contact Lisa Levine, MD, MSCE
Phone 215-283-7373
Email lisa.levine@pennmedicine.upenn.edu
Status Recruiting
Phase N/A
Start date April 13, 2023
Completion date June 30, 2027
View Details
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