NCT01801410View on ClinicalTrials.gov

Induction With Foley OR Misoprostol (INFORM) Study

PHASE3CompletedINTERVENTIONAL
Enrollment

602

Participants

Timeline

Start Date

December 31, 2013

Primary Completion Date

June 30, 2015

Study Completion Date

June 30, 2015

Conditions
Pre-eclampsiaFetus or Newborn; Effects of Induction of Labor
Interventions
DEVICE

Foley Catheter

Transcervical Foley catheter (silicone, size 18F with 30ml balloon)

DRUG

Misoprostol

25mcg every 2 hours for maximum of 12 doses

Trial Locations (2)

Unknown

Daga Memorial Women's Hospital, Nagpur

Government Medical College (GMC), Nagpur

All Listed Sponsors
collaborator

Gynuity Health Projects

OTHER

collaborator

Government Dental College and Hospital, India

OTHER_GOV

collaborator

Daga Memorial Women's Hospital, Nagpur, India

OTHER

lead

University of Liverpool

OTHER

NCT01801410 - Induction With Foley OR Misoprostol (INFORM) Study | Biotech Hunter | Biotech Hunter