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
| Type | Name | Description |
|---|---|---|
| DEVICE | Foley balloon | Foley balloon for induction of labor |
| DRUG | Oxytocin | Pitocin 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.