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Comparison of Oral Versus Vaginal Misoprostol for Labour Induction at Term

NCT05957666 · Status: UNKNOWN · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 176

Last updated 2023-07-24

No results posted yet for this study

Summary

A randomised control trial to compare oral and vaginal misoprostol for induction of labour in term patients.The objective is to determine whether use of standardised vaginal misoprostol regimen will result in decreased cesaerean section rate among women with bishop score of lessthan or equal to 6 who require induction of labpour at term compared to oral misoprostol regimen.

Conditions

  • Induction of Labour With Misoprostol

Interventions

DRUG

Misoprostol Oral Tablet

oral misoprostol 50 microgram repeated after 6 hours if required

DRUG

vaginal misoprostol

vaginal misoprostol 50 microgram repeated after 6 hours if required

Sponsors & Collaborators

  • Services Institute of Medical Sciences, Pakistan

    lead OTHER_GOV

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-06-16
Primary Completion
2023-12-16
Completion
2023-12-16

Countries

  • Pakistan

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 NCT05957666 on ClinicalTrials.gov