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Patient Satisfaction of Cervical Ripening in an Outpatient Setting

NCT01605474 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 800

Last updated 2012-05-25

No results posted yet for this study

Summary

This study examines whether outpatient pre-induction cervical ripening improves patient satisfaction and is safe and effective.

Conditions

  • Pregnancy

Interventions

OTHER

Patient discharged home after foley bulb placement.

The patient will be discharged home after fetal status is evaluated and noted to be reassuring. A 16 French foley bulb insufflated with 30 cc of normal saline will be placed and secured to the patient's inner thigh.

OTHER

Inpatient

The patients will not be discharged home after assessment and placement of the foley catheter.

Sponsors & Collaborators

  • Cedars-Sinai Medical Center

    lead OTHER

Principal Investigators

  • Tania Esaoff, MD · Cedars-Sinai Medical Center, Department of Obstetrics and Gynecology, Division of Maternal Fetal Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-04-30
Primary Completion
2014-07-31

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 NCT01605474 on ClinicalTrials.gov