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Inpatient Versus Outpatient Foley Cervical Ripening Study

NCT03725397 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2023-02-22

No results posted yet for this study

Summary

To compare the efficacy and safety of cervical ripening with transcervical Foley catheter in inpatient vs outpatient setting

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".

Sponsors & Collaborators

  • Yale University

    lead OTHER

Principal Investigators

  • Katherine Kohari, MD · Yale University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-01-08
Primary Completion
2022-06-27
Completion
2022-06-27

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03725397 on ClinicalTrials.gov