NCT00393731View on ClinicalTrials.gov

A Randomized, Control Trial for Preinduction Cervical Ripening

PHASE2CompletedINTERVENTIONAL
Enrollment

540

Participants

Timeline

Start Date

January 31, 2004

Primary Completion Date

August 31, 2007

Study Completion Date

August 31, 2007

Conditions
Labor, Induced
Interventions
DRUG

Misoprostol

DRUG

oxytocin

Trial Locations (1)

77026

Lyndon B. Johnson Hospital, Houston

All Listed Sponsors
lead

The University of Texas Health Science Center, Houston

OTHER

NCT00393731 - A Randomized, Control Trial for Preinduction Cervical Ripening | Biotech Hunter | Biotech Hunter