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Comparison of Two Regimens of Misoprostol for Second Trimester Medical Termination of Pregnancy

NCT00401440 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 185

Last updated 2010-03-12

No results posted yet for this study

Summary

The hypothesis of the study is that the induction abortion interval time will be significantly shorter in the group receiving vaginal misoprostol every six hours in comparison to the group who are receiving vaginal misoprostol every twelve hours.

Conditions

  • Induced Abortion

Interventions

DRUG

Misoprostol

400 microgram vaginal misoprostol tablet will be applied every 6 hours with a maximum of 4 doses

DRUG

Misoprostol

400 microgram vaginal misoprostol tablet will be applied every 12 hours with a maximum of 4 doses

Sponsors & Collaborators

  • Nilratan Sircar Medical College

    lead OTHER_GOV

Principal Investigators

  • Snehamay Chaudhuri, MBBS,MD,DNB · Nilratan Sircar Medical College , 138,AJC Bose Road , Kolkata,700014,West Bengal , India.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
14 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-01-31
Primary Completion
2008-09-30
Completion
2008-09-30

Countries

  • India

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 NCT00401440 on ClinicalTrials.gov