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NCT04755218 · ClinicalTrials.gov registry record

Labor Induction With Oral Versus Vaginal Misoprostol

A clinical trial of Pregnancy and Labor, Induced, sponsored by University of Texas Southwestern Medical Center.

Completed
Registry status
2,546
Enrollment target
1
Study location

NCT04755218 is a study of Pregnancy and Labor, Induced that has completed, run by University of Texas Southwestern Medical Center. The registered enrollment target is 2,546 participants, above the 859-participant average among 191 other Pregnancy trials with a reported enrollment target (196% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT04755218, a study of Pregnancy and Labor, Induced, has completed, sponsored by University of Texas Southwestern Medical Center.

COMPLETED
Registry status
2,546 participants
Enrollment target
1
Study location

Study Summary

This study will compare vaginal and oral misoprostol, to determine whether a vaginal misoprostol regimen achieves a higher vaginal delivery rate in a real-world, high-volume setting, and whether this regimen reduces time and oxytocin need on a high-volume Labor and Delivery unit at Parkland Hospital. Our primary hypothesis is that among women with singleton, term pregnancies, cervical dilation 2cm or less, and indicated labor induction, the rate of vaginal delivery is significantly increased when a standardized vaginal misoprostol regimen is used, compared with a standardized oral misoprostol regimen.

Conditions Studied

Study Locations (1)

Texas

  • Parkland Health and Hospital Systems - Dallas

Trial Details

FieldValue
Enrollment Target 2,546 participants
Start Date 2021-05-24
Est. Completion 2023-07-07

What the Registry Record Tells You About NCT04755218

The ClinicalTrials.gov registry entry for NCT04755218 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 2,546 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 859-participant average among 191 other Pregnancy trials with a reported enrollment target (196% higher). The listed sponsor is University of Texas Southwestern Medical Center, which has 837 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Pregnancy appearing as the primary indexed condition, and to 0 interventions.

NCT04755218 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT04755218 about?

NCT04755218 is a clinical study titled "Labor Induction With Oral Versus Vaginal Misoprostol". This study will compare vaginal and oral misoprostol, to determine whether a vaginal misoprostol regimen achieves a higher vaginal delivery rate in a real-world, high-volume setting, and whether this regimen reduces time and oxytocin need on a high-volume Labor and Delivery unit at Parkland Hospital...

What is the current status of trial NCT04755218?

This trial is currently completed. The enrollment target is 2,546 participants. The study started on 2021-05-24. Estimated completion is 2023-07-07.

What conditions does trial NCT04755218 study?

This clinical trial studies the following conditions: Pregnancy, Labor, Induced.

Who is sponsoring clinical trial NCT04755218?

This trial is sponsored by University of Texas Southwestern Medical Center, which has 837 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04755218 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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