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NCT07006896 · ClinicalTrials.gov registry record · NA
Induction of Labor After Cesarean Using Foley Alone vs. Concurrent Foley and Oxytocin
A NA study of Cesarean Delivery and Labor Induction, sponsored by University of Pennsylvania.
- Recruiting
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT07006896 is a NA study of Cesarean Delivery and Labor Induction that is actively recruiting participants, run by University of Pennsylvania. The registered enrollment target is 100 participants, below the 3,473-participant average among 10 other Cesarean Delivery trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07006896, a NA study of Cesarean Delivery and Labor Induction, is actively recruiting participants, sponsored by University of Pennsylvania.
- RECRUITING
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
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 Studied
Interventions
- DRUG Oxytocin
- DEVICE Foley balloon
Study Locations (1)
Pennsylvania
- Hospital of the University of Pennsylvania - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2025-07-10 |
| Est. Completion | 2027-05-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07006896
The ClinicalTrials.gov registry entry for NCT07006896 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,473-participant average among 10 other Cesarean Delivery trials with a reported enrollment target (97% lower). The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Cesarean Delivery appearing as the primary indexed condition, and to 2 interventions - of which Oxytocin is the first listed.
NCT07006896 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT07006896 about?
NCT07006896 is a clinical study titled "Induction of Labor After Cesarean Using Foley Alone vs. Concurrent Foley and Oxytocin". 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 sta...
What is the current status of trial NCT07006896?
This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2025-07-10. Estimated completion is 2027-05-01.
What conditions does trial NCT07006896 study?
This clinical trial studies the following conditions: Cesarean Delivery, Labor Induction.
What interventions are being tested in trial NCT07006896?
The interventions under investigation include: Oxytocin (DRUG), Foley balloon (DEVICE).
Who is sponsoring clinical trial NCT07006896?
This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07006896 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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