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Comparitive Study of Two Misoprostol Regimen in Early Pregnancy Termination

NCT01508143 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 41

Last updated 2012-10-02

No results posted yet for this study

Summary

The aim of this study is to compare two misoprostol regimen in pregnancy termination.

Conditions

  • Termination

Interventions

DRUG

Misoprostol 400 micrograms

Misoprostol 400 micrograms each 6 hours for 8 dose

DRUG

Misoprostol 800 micrograms

Misoprostol 800 micrograms each 12 hours for 4 doses

Sponsors & Collaborators

  • Hormozgan University of Medical Sciences

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-01-31
Primary Completion
2012-09-30
Completion
2012-09-30

Countries

  • Iran

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 NCT01508143 on ClinicalTrials.gov