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Efficacy and Safety of Titrated Oral Misoprostol Solution for Labor Induction at Term

NCT01070472 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 250

Last updated 2013-12-10

No results posted yet for this study

Summary

The purpose of this study is to determine whether a titrated solution of oral Misoprostol is safe and effective at inducing labor at term, regardless of Bishop Score.

Conditions

  • Labor Induction at Term

Interventions

DRUG

Misoprostol

titrated oral misoprostol solution

Sponsors & Collaborators

  • University of Manitoba

    lead OTHER

Principal Investigators

  • debbie J Robinson, MD FRCSC · University of Manitoba

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
44 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2011-06-30
Completion
2011-06-30

Countries

  • Canada

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 NCT01070472 on ClinicalTrials.gov