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Randomized Trial Comparing Misoprostol and Foley Bulb for Labor Induction in the Preterm Gestation

NCT00325026 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 130

Last updated 2012-03-02

No results posted yet for this study

Summary

The purpose of this study is to compare the time to delivery of two different cervical ripening methods on the preterm gestation.

Conditions

  • Premature Birth
  • Cervical Ripening

Interventions

DRUG

Misoprostol

DEVICE

Foley bulb

Sponsors & Collaborators

  • University of Florida

    lead OTHER

Principal Investigators

  • Keri a Baacke, MD · University of Florida

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
2005-04-30
Completion
2007-04-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs

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 NCT00325026 on ClinicalTrials.gov