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Failure of Vaginal Delivery After Induction

NCT02758340 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 335

Last updated 2016-11-29

No results posted yet for this study

Summary

The study will compare the number of women who deliver vaginally after artificial initiation of labor pains(i.e. induction of labor) by two methods. Half of the women would receive tablet misoprostol vaginally and the other half would receive tablet misoprostol and foley's balloon catheter both.

Conditions

  • Labor Pain

Interventions

DRUG

Misoprostol

Women would be given misoprostol tablet by mouth

DEVICE

foley's balloon catheter

foley's balloon catheter would be inserted through vagina into cervix.

Sponsors & Collaborators

  • Karachi Medical and Dental College

    lead OTHER

Principal Investigators

  • samia husain, MBBS · Karachi Medical and Dental College

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2016-04-30
Primary Completion
2016-11-30
Completion
2016-11-30

Countries

  • Pakistan

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 NCT02758340 on ClinicalTrials.gov