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NCT04492072 · ClinicalTrials.gov registry record · NA
Misoprostol With Mechanical Dilation Versus Oxytocin With Mechanical Dilation for High-risk Pregnancy Inductions
A NA study of Cesarean Section and High Risk Pregnancy, sponsored by Thomas Jefferson University.
- Completed
- Registry status
- NA
- Development phase
- 150
- Enrollment target
- 1
- Study location
NCT04492072 is a NA study of Cesarean Section and High Risk Pregnancy that has completed, run by Thomas Jefferson University. The registered enrollment target is 150 participants, roughly in line with the 160-participant average among 14 other Cesarean Section trials with a reported enrollment target. The trial reports 1 study location across 1 state.
The verdict
NCT04492072, a NA study of Cesarean Section and High Risk Pregnancy, has completed, sponsored by Thomas Jefferson University.
- COMPLETED
- Registry status
- NA
- Development phase
- 150 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to specifically investigate whether oxytocin and mechanical dilation decreases the rate of cesarean section compared to misoprostol and mechanical dilation for pregnancies at risk of fetal compromise
Conditions Studied
Interventions
- DRUG Oxytocin
- DRUG Misoprostol
Study Locations (1)
Pennsylvania
- Thomas Jefferson University Hospital - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2020-08-17 |
| Est. Completion | 2022-05-26 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04492072
The ClinicalTrials.gov registry entry for NCT04492072 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 160-participant average among 14 other Cesarean Section trials with a reported enrollment target. The listed sponsor is Thomas Jefferson University, which has 292 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Cesarean Section appearing as the primary indexed condition, and to 2 interventions - of which Oxytocin is the first listed.
NCT04492072 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT04492072 about?
NCT04492072 is a clinical study titled "Misoprostol With Mechanical Dilation Versus Oxytocin With Mechanical Dilation for High-risk Pregnancy Inductions". The purpose of this study is to specifically investigate whether oxytocin and mechanical dilation decreases the rate of cesarean section compared to misoprostol and mechanical dilation for pregnancies at risk of fetal compromise
What is the current status of trial NCT04492072?
This trial is currently completed. It is a NA study. The enrollment target is 150 participants. The study started on 2020-08-17. Estimated completion is 2022-05-26.
What conditions does trial NCT04492072 study?
This clinical trial studies the following conditions: Cesarean Section, High Risk Pregnancy, Oxytocin, Misoprostol.
What interventions are being tested in trial NCT04492072?
The interventions under investigation include: Oxytocin (DRUG), Misoprostol (DRUG).
Who is sponsoring clinical trial NCT04492072?
This trial is sponsored by Thomas Jefferson University, which has 292 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04492072 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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