NCT03725397View on ClinicalTrials.gov

Inpatient Versus Outpatient Foley Cervical Ripening Study

NACompletedINTERVENTIONAL
Enrollment

54

Participants

Timeline

Start Date

January 8, 2019

Primary Completion Date

June 27, 2022

Study Completion Date

June 27, 2022

Conditions
Induced; Birth
Interventions
BEHAVIORAL

Outpatient

The offered (studied) intervention will be allowing the women with a transcervical Foley catheter in place to spend the night at home.

BEHAVIORAL

Inpatient

"Women with a transcervical Foley catheter to be admitted to the hospital overnight which has been a standard of care."

Trial Locations (2)

06511

Yale New Haven Hospital- St. Raphael, New Haven

06520

Yale New Haven Hospital, York Street Campus, New Haven

All Listed Sponsors
lead

Yale University

OTHER

NCT03725397 - Inpatient Versus Outpatient Foley Cervical Ripening Study | Biotech Hunter | Biotech Hunter