Clinical Trials Directory

Trials / Completed

CompletedNCT01508143

Comparitive Study of Two Misoprostol Regimen in Early Pregnancy Termination

A Comparative Study of Vaginal Misoprostol Two Dosing Regimen for First Trimester Pregnancy Termination in Patients Admitted at Bandarabbas in Shariati Hospital in 2009

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
41 (actual)
Sponsor
Hormozgan University of Medical Sciences · Academic / Other
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

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

Detailed description

Studies on determining the optimal dosage for misoprostol in pregnancy termination are continuing and still there is no evidence for ideal misoprostol regimen for pregnancy termination. The aim of this study is to compare two misoprostol regimen in pregnancy termination.

Conditions

Interventions

TypeNameDescription
DRUGMisoprostol 400 microgramsMisoprostol 400 micrograms each 6 hours for 8 dose
DRUGMisoprostol 800 microgramsMisoprostol 800 micrograms each 12 hours for 4 doses

Timeline

Start date
2012-01-01
Primary completion
2012-09-01
Completion
2012-09-01
First posted
2012-01-11
Last updated
2012-10-02

Locations

1 site across 1 country: Iran

Source: ClinicalTrials.gov record NCT01508143. Inclusion in this directory is not an endorsement.