Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT06199154
EARLY_PHASE1

Induction of Labor in Morbidly Obese Patients

Sponsor: University of Maryland, Baltimore

View on ClinicalTrials.gov

Summary

The goal of this randomized control trial is to compare different doses of Misoprostol (25 mcg vs 50 mcg) in induction of labor (IOL) in morbidly obese patients with BMI \>40. It is known that morbid obesity is a risk factor for failed IOL and ultimately cesarean delivery (CD.) If the rates of vaginal delivery in this population can improve, then surgical morbidity can be reduced in these patients.

Official title: Induction of Labor in Morbidly Obese Patients: Comparison of 50 mcg and 25 mcg Misoprostol - A Randomized Control Trial

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

162

Start Date

2024-07-15

Completion Date

2026-10

Last Updated

2025-07-03

Healthy Volunteers

No

Interventions

DRUG

Misoprostol

Participants will receive with 25 mcg or 50 mcg vaginal misoprostol every 4 hours.

Locations (1)

University of Maryland Medical Center

Baltimore, Maryland, United States