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
| Type | Name | Description |
|---|---|---|
| DRUG | misoprostol | comparison of orally administered 600mcg of misoprostol to either sublingually administered 400mcg or Manual Vacuum Aspiration (MVA) |
| PROCEDURE | MVA | comparison 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.