Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07006896

Induction of Labor After Cesarean Using Foley Alone vs. Concurrent Foley and Oxytocin

Labor Induction After Cesarean: A Randomized Trial Of Cervical Balloon With or Without Oxytocin

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
University of Pennsylvania · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

A randomized trial of patients undergoing a term (≥37 weeks) induction of labor with a history of one prior Cesarean delivery, wherein the provider intends to use a Foley catheter for cervical ripening. The investigators will be comparing Foley alone with concurrent Foley and Oxytocin use at the start of the induction. With this trial, the investigators aim to test our central hypothesis that concurrent Foley and Oxytocin will decrease time to delivery without increasing risks, compared to Foley alone.

Conditions

Interventions

TypeNameDescription
DEVICEFoley balloonFoley balloon for induction of labor
DRUGOxytocinPitocin for induction of labor

Timeline

Start date
2025-07-10
Primary completion
2027-05-01
Completion
2027-05-01
First posted
2025-06-05
Last updated
2025-07-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07006896. Inclusion in this directory is not an endorsement.