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NCT05782816 · ClinicalTrials.gov registry record · Phase 4
Low-Dose Versus High-Dose Oxytocin Dosing for Induction and Augmentation of Labor
A Phase 4 study of Labor Long, sponsored by The University of Texas Medical Branch, Galveston.
- Completed
- Registry status
- Phase 4
- Development phase
- 170
- Enrollment target
- 1
- Study location
NCT05782816 is a Phase 4 study of Labor Long that has completed, run by The University of Texas Medical Branch, Galveston. The registered enrollment target is 170 participants. The trial reports 1 study location across 1 state.
The verdict
NCT05782816, a Phase 4 study of Labor Long, has completed, sponsored by The University of Texas Medical Branch, Galveston.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 170 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to compare oxytocin infusion rates for induction and augmentation of labor in nulliparous women. The main question\[s\] it aims to answer are: * Does a high dose oxytocin infusion protocol affect length of induction to delivery interval? * Does a high dose oxytocin infusion protocol affect mode of delivery? * Does a high dose oxytocin infusion protocol affect maternal and neonatal outcomes? Participants will be randomized to either low- or high-dose oxytocin groups: * The low dose group will receive an infusion to start at 2 milli-units/min and will be increased by 2 milli-units/min every 20 minutes. The maximum rate of infusion is 40 milli-units/min. * The high dose group will receive an infusion to start at 6 milli-units/min and will be increased by 6 milli-units/min every 20 minutes. Maximum rate of infusion is 40 milli-units/min.
Conditions Studied
Interventions
- DRUG Oxytocin (Low dose)
- DRUG Oxytocin (High dose)
Study Locations (1)
Texas
- University of Texas Medical Branch - Galveston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 170 participants |
| Start Date | 2023-04-17 |
| Est. Completion | 2025-06-24 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05782816
The ClinicalTrials.gov registry entry for NCT05782816 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 170 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Medical Branch, Galveston, which has 203 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Labor Long appearing as the primary indexed condition, and to 2 interventions - of which Oxytocin (Low dose) is the first listed.
NCT05782816 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT05782816 about?
NCT05782816 is a clinical study titled "Low-Dose Versus High-Dose Oxytocin Dosing for Induction and Augmentation of Labor". The goal of this clinical trial is to compare oxytocin infusion rates for induction and augmentation of labor in nulliparous women. The main question\[s\] it aims to answer are: * Does a high dose oxytocin infusion protocol affect length of induction to delivery interval? * Does a high dose oxytoci...
What is the current status of trial NCT05782816?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 170 participants. The study started on 2023-04-17. Estimated completion is 2025-06-24.
What conditions does trial NCT05782816 study?
This clinical trial studies the following conditions: Labor Long.
What interventions are being tested in trial NCT05782816?
The interventions under investigation include: Oxytocin (Low dose) (DRUG), Oxytocin (High dose) (DRUG).
Who is sponsoring clinical trial NCT05782816?
This trial is sponsored by The University of Texas Medical Branch, Galveston, which has 203 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05782816 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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