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Foley Catheter Versus Cervidil for Induction of Labor at Term

NCT01402050 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 376

Last updated 2020-03-02

Study results available
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Summary

OBJECTIVE: To assess the efficacy of transcervical Foley catheter compared to controlled release prostaglandin (Cervidil™) for cervical ripening in term and near term women presenting for labor induction.

HYPOTHESIS: In term and near term women presenting for labor induction, transcervical Foley catheter will decrease the mean time from induction to delivery by six hours compared to controlled release prostaglandin (Cervidil™).

Conditions

  • Labor Induction

Interventions

DRUG

CERVIDIL (Dinoprostone)

INDUCTION OF LABOR

DEVICE

FOLEY BALLOON

INDUCTION OF LABOR

Sponsors & Collaborators

  • Pediatrix

    lead OTHER

Principal Investigators

  • Monique G Lin, MD · Obstetrix Medical Group

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2010-06-30
Primary Completion
2014-11-30
Completion
2015-02-28

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 NCT01402050 on ClinicalTrials.gov