NCT02639429View on ClinicalTrials.gov

Cervical Ripening for Obese Women: A Randomized, Comparative Effectiveness Trial

PHASE4CompletedINTERVENTIONAL
Enrollment

236

Participants

Timeline

Start Date

January 31, 2016

Primary Completion Date

June 24, 2018

Study Completion Date

June 24, 2018

Conditions
ObesityLabor InductionCesarean Delivery
Interventions
DRUG

Vaginal Misoprostol

DEVICE

Foley Balloon + Vaginal Misoprostol

Trial Locations (1)

77030

The University of Texas Health Science Center, Houston

All Listed Sponsors
lead

The University of Texas Health Science Center, Houston

OTHER

NCT02639429 - Cervical Ripening for Obese Women: A Randomized, Comparative Effectiveness Trial | Biotech Hunter | Biotech Hunter