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Comparing 30mL Single Versus 80mL Double Balloon Catheters for Pre-induction Cervical Ripening

NCT02344459 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 105

Last updated 2015-01-26

No results posted yet for this study

Summary

The purpose of this study is to perform a randomized controlled trial to compare the efficacy of 80mL double balloon catheter versus a 30mL single catheter balloon for pre-induction cervical ripening by evaluating the change in Bishop score.

Conditions

  • Pre-induction Cervical Ripening

Interventions

DEVICE

mechanical pre-induction cervical ripening

The balloon catheters have been used to provide mechanical dilation to the cervix as a method of pre-induction cervical ripening.

Sponsors & Collaborators

Principal Investigators

  • Kara K Hoppe, DO · University of Washington

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2013-11-30
Completion
2013-11-30

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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 NCT02344459 on ClinicalTrials.gov