NCT03045939View on ClinicalTrials.gov

Cervical Ripening With the Double Balloon Device for 6 Hours Compared With 12 Hours

NAUnknownINTERVENTIONAL
Enrollment

200

Participants

Timeline

Start Date

March 1, 2017

Primary Completion Date

February 1, 2019

Study Completion Date

March 1, 2019

Conditions
Induction of LaborUnfavorable Cervix
Interventions
DEVICE

cervical ripening device

insertion of the double balloon device for 12 hours (standard care) vs 6 hours, following oxytocin IV infusion according local protocol guidelines as mentioned above

Trial Locations (1)

Unknown

RECRUITING

Bnai Zion Mc, Haifa

Sponsors
All Listed Sponsors
lead

Bnai Zion Medical Center

OTHER_GOV