Clinical Trials Directory

Trials / Completed

CompletedNCT00670761

Misoprostol for the Treatment of Incomplete Abortion

Misoprostol for the Treatment of Incomplete Abortion: Comparison of Treatment Options

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
720 (actual)
Sponsor
Gynuity Health Projects · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

This randomized study will examine the efficacy, safety and acceptability of misoprostol for treatment of incomplete abortion. Women diagnosed with incomplete abortion will be randomized to receive one of the following regimens: In Tanzania and Mozambique: 1. 600 mcg of oral misoprostol in one dose, or 2. Standard surgical treatment (MVA) In Moldova and Madagascar: 1. 600 mcg of oral misoprostol in one dose, or 2. 400 mcg of sublingual misoprostol in one dose. In Burkina Faso and Vietnam: 1\. 400 mcg of sublingual misoprostol in one dose. We hypothesize that treatment of incomplete abortion with either 400 mcg sublingual misoprostol, 600 mcg oral misoprostol or MVA are equally effective in evacuating the uterus.

Conditions

Interventions

TypeNameDescription
DRUGmisoprostolcomparison of orally administered 600mcg of misoprostol to either sublingually administered 400mcg or Manual Vacuum Aspiration (MVA)
PROCEDUREMVAcomparison of orally administered 600mcg of misoprostol to either sublingually administered 400mcg or Manual Vacuum Aspiration (MVA)

Timeline

Start date
2004-07-01
Primary completion
2010-04-01
Completion
2010-12-01
First posted
2008-05-02
Last updated
2016-07-27

Locations

6 sites across 5 countries: Burkina Faso, Madagascar, Moldova, Mozambique, Tanzania

Source: ClinicalTrials.gov record NCT00670761. Inclusion in this directory is not an endorsement.