Actively Recruiting
Induction of Labor After Cesarean Using Foley Alone vs. Concurrent Foley and Oxytocin
Led by University of Pennsylvania · Updated on 2025-07-18
100
Participants Needed
1
Research Sites
94 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
Official Title
Induction of Labor After Cesarean Using Foley Alone vs. Concurrent Foley and Oxytocin
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Eligible for induction of labor
- Live singleton gestation 537 weeks
- History of 1 cesarean delivery
- 518 years of age
- Cephalic presentation
- Intact membranes
- English or Spanish speaking (Able to read/understand consent and instructions)
- Cervical dilation <3cm and Bishop score <8
You will not qualify if you...
- More than 1 prior Cesarean delivery
- Known chorioamnionitis
- Major fetal anomaly
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hospital of the University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19146
Actively Recruiting
Research Team
H
Hannah Foster, MD, MAUB
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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