Clinical Trials Directory

Trials / Completed

CompletedNCT01387256

Comparing Two Regimens for Medical Abortion: Mifepristone + Misoprostol Versus Misoprostol Alone

Comparing Two Regimens for Medical Abortion: Mifepristone + Misoprostol Versus Misoprostol Alone-3 Hour Intervals

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
441 (actual)
Sponsor
Gynuity Health Projects · Academic / Other
Sex
Female
Age
Healthy volunteers
Accepted

Summary

This double blinded, placebo-controlled randomized trial will compare the safety, efficacy and acceptability of two medical abortion regimens up to 63 days since last Menstrual Period (LMP) in Tunisia and Vietnam. The first regimen will include a 200 mg oral dose of mifepristone followed by 800 mcg buccal misoprostol. The second regimen will include two 800 mcg doses of buccal misoprostol three hours apart. All drugs are administered AT home by the participant.

Conditions

Interventions

TypeNameDescription
DRUGmedical abortionpregnancy termination with drugs

Timeline

Start date
2009-05-01
Primary completion
2010-07-01
Completion
2010-07-01
First posted
2011-07-04
Last updated
2011-07-20

Locations

2 sites across 2 countries: Tunisia, Vietnam

Source: ClinicalTrials.gov record NCT01387256. Inclusion in this directory is not an endorsement.