NCT03489798View on ClinicalTrials.gov

Comparison of Two Protocols of Misoprostol (PGE1) and the Rate of Cesarean Section Due to Failed Induction.

NACompletedINTERVENTIONAL
Enrollment

310

Participants

Timeline

Start Date

April 5, 2018

Primary Completion Date

May 31, 2018

Study Completion Date

September 15, 2018

Conditions
Induction of Labor
Interventions
PROCEDURE

6 misoprostol

Up to 6 doses of 25ug of misoprostol applied every 6 hours. End point is cervical Bishop score \> 6.

PROCEDURE

3 misoprostol

Up to 3 doses of 25ug of misoprostol applied every 6 hours. End point is cervical Bishop score \> 6.

Trial Locations (1)

Unknown

Saint Thomas Maternity Hospital, Panama City

All Listed Sponsors
collaborator

Sistema Nacional de Investigadores de Panamá

UNKNOWN

lead

Saint Thomas Hospital, Panama

OTHER

NCT03489798 - Comparison of Two Protocols of Misoprostol (PGE1) and the Rate of Cesarean Section Due to Failed Induction. | Biotech Hunter | Biotech Hunter