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

NCT07006896 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2025-07-18

No results posted yet for this study

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

  • Labor Induction
  • Cesarean Delivery

Interventions

DEVICE

Foley balloon

Foley balloon for induction of labor

DRUG

Oxytocin

Pitocin for induction of labor

Sponsors & Collaborators

Principal Investigators

  • Lisa Levine, MD MSCE · University of Pennsylvania

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-07-10
Primary Completion
2027-05-01
Completion
2027-05-01

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07006896 on ClinicalTrials.gov