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Labor Induction With Oral Versus Vaginal Misoprostol

NCT04755218 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2546

Last updated 2024-04-05

No results posted yet for this 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

  • Pregnancy
  • Labor, Induced

Sponsors & Collaborators

  • University of Texas Southwestern Medical Center

    lead OTHER

Principal Investigators

  • Emily H Adhikari, MD · University of Texas Southwestern Medical Center

Eligibility

Min Age
10 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-05-24
Primary Completion
2022-09-18
Completion
2023-07-07

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04755218 on ClinicalTrials.gov