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RECRUITING Phase 4

Oxytocin/Foley vs. Oxytocin for Induction in Patients With PPROM

NCT07119398 · View on ClinicalTrials.gov ↗

Study Summary

Data on the optimal mode of labor induction after preterm prelabor rupture of membranes (PPROM) is lacking. Studies have shown no difference between oxytocin and misoprostol use for labor induction in this cohort (1). The preponderance of evidence from term pregnancies suggests that Foley catheter coupled with oxytocin is better than oxytocin alone, with a higher rate of delivery within 24 hours when a Foley catheter followed by oxytocin is compared to oxytocin alone. However, the use of a Foley catheter has not been evaluated in prospective studies on patients with PPROM.

Conditions Studied

Interventions

  • COMBINATION_PRODUCT Oxytocin plus Foley Catheter
  • DRUG Oxytocin

Study Locations (1)

Virginia

  • Sentara Norfolk General Hospital — Norfolk

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2025-07-14
Est. Completion 2026-12-30
Phase Phase 4

Sponsor

Eastern Virginia Medical School

71 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07119398

The ClinicalTrials.gov registry entry for NCT07119398 describes a study currently listed as recruiting. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eastern Virginia Medical School, which has 71 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Preterm PROM (Pregnancy) appearing as the primary indexed condition, and to 2 interventions — of which Oxytocin plus Foley Catheter is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07119398 reports 1 study location spanning 1 distinct geographic area — top geographies include Virginia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07119398 about?

NCT07119398 is a clinical study titled "Oxytocin/Foley vs. Oxytocin for Induction in Patients With PPROM". Data on the optimal mode of labor induction after preterm prelabor rupture of membranes (PPROM) is lacking. Studies have shown no difference between oxytocin and misoprostol use for labor induction in this cohort (1). The preponderance of evidence from term pregnancies suggests that Foley catheter c...

What is the current status of trial NCT07119398?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 80 participants. The study started on 2025-07-14. Estimated completion is 2026-12-30.

What conditions does trial NCT07119398 study?

This clinical trial studies the following conditions: Preterm PROM (Pregnancy). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07119398?

The interventions under investigation include: Oxytocin plus Foley Catheter (COMBINATION_PRODUCT), Oxytocin (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07119398?

This trial is sponsored by Eastern Virginia Medical School, which has 71 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07119398 being conducted?

This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial