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Clinical Trials/NCT02168881
NCT02168881
Unknown
Not Applicable

Oral Misoprostol Versus Vaginal Dinoprostone For Induction Of Labour: A Randomized Controlled Clinical Trial

Ain Shams University1 site in 1 country342 target enrollmentMay 2014

Overview

Phase
Not Applicable
Intervention
Misoprostol
Conditions
Labour Induction
Sponsor
Ain Shams University
Enrollment
342
Locations
1
Primary Endpoint
induction delivery time
Last Updated
11 years ago

Overview

Brief Summary

This study is to compare between oral misoprostol in solution and vaginal dinoprostone in induction of labour in primiparous women with singleton pregnancy as regards efficiency and safety to both mother and fetus.

Registry
clinicaltrials.gov
Start Date
May 2014
End Date
January 2016
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marwan Elkady

Dr

Ain Shams University

Eligibility Criteria

Inclusion Criteria

  • Primigravida

Exclusion Criteria

  • Scarred uterus
  • Macrosomia

Arms & Interventions

misoprostol

oral misoprostol in solution 25 microgram every 2 hours

Intervention: Misoprostol

dinoprostone

3 mgs dinoprostone vaginally every six hours

Intervention: Dinoprostone

Outcomes

Primary Outcomes

induction delivery time

Time Frame: 2 hourly

Study Sites (1)

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