DRUG
Misoprostol
25 mcg vaginally every 6 hours
Status
Recruiting
Phase
Phase 3
Enrollment
281
Locations
2
Results
Not posted
Publications
0
Study summary
This is a randomized controlled trial examining whether the use of misoprostol or pitocin, in combination with a foley catheter, is more effective at inducing labor in patients with a gravid BMI that is considered obese.
This randomized controlled trial will include patients with a BMI greater than 30 at the time of admission for their induction of labor. Patients will be randomized to either misoprostol or Pitocin to begin induction of labor, alongside the standard foley catheter, and the primary outcome of interest will be length of time from start of induction until delivery.
Interventions
DRUG
25 mcg vaginally every 6 hours
DRUG
3-6 mL intravenously every hour
Timeline
First posted
Feb 14, 2024
Study start
Jul 2, 2024
Primary completion
Aug 2026
Study completion
Aug 2026
Results posted
Not reported
Registry updated
Jul 24, 2026
Outcomes
Time from induction to delivery
Time frame · start of induction until delivery
Simple measure calculating time from start of induction until delivery of neonate.
Delivery outcome
Time frame · at delivery
Simple determination whether patient had a vaginal delivery or delivered by cesarean section.
Eligibility
Inclusion Criteria: \- Pregnant patient presenting to labor \& delivery for induction of labor with a BMI \> = 30 Exclusion Criteria: \- Pregnant patient presenting to labor \& delivery for induction of labor with BMI \< 30
Study locations
United States. Showing up to 24 locations stored in the fast local snapshot.
Mount Sinai Hospital
New York, New York, United States
Bronx Care Health System
The Bronx, New York, United States
Publications
No PMID-linked publications were present in this registry snapshot.
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