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Trial of Foley Catheter With and Without Extra-Amniotic Saline Infusion for Labor Induction

NCT00442663 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 170

Last updated 2007-04-24

No results posted yet for this study

Summary

The purpose of this study is to compare the efficacy of a transcervical Foley catheter with and without extra-amniotic saline infusion (EASI) for priming the cervix for labor.

Conditions

  • Labor Induction
  • Cervical Ripening

Interventions

DEVICE

Transcervical Foley Catheter

DEVICE

Transcervical Foley Catheter with an EASI

Sponsors & Collaborators

  • University of Alabama at Birmingham

    lead OTHER

Principal Investigators

  • Monique G Lin, MD · University of Alabama at Birmingham

  • George Lu, MD · Obstetrix Medical Group of Kansas City

  • Patrick S Ramsey, MD, MSPH · University of Alabama at Birmingham

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
15 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2003-06-30
Completion
2005-12-31

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 NCT00442663 on ClinicalTrials.gov