NCT00386867View on ClinicalTrials.gov

A Randomized Trial of Buccal Compared to Oral Misoprostol Following Mifepristone for Medical Abortion up to 63 Days LMP

NACompletedINTERVENTIONAL

Enrollment

1,200

Participants

Timeline

Start Date

October 31, 2006

Study Completion Date

March 31, 2007

Conditions

Abortion, Induced

Interventions

DRUG

800 mcg misoprostol via oral or buccal administration

Trial Locations (8)

Unknown

Family Planning Associates Medical Group, Chicago

Planned Parenthood League of Massachusetts (Boston clinic), Boston

Columbia University Medical Center, Division of Obstetrics & Gynecology, New York

Institute for Urban Family Health, New York

Parkmed, New York

University of Pittsburgh, Division of Obstetrics, Gynecology and Reproductive Sciences, Pittsburgh

Whole Women's Health, Austin

Planned Parenthood, Waco

All Listed Sponsors

lead

Gynuity Health Projects

OTHER

NCT00386867 - A Randomized Trial of Buccal Compared to Oral Misoprostol Following Mifepristone for Medical Abortion up to 63 Days LMP | Biotech Hunter | Biotech Hunter