NCT00466999View on ClinicalTrials.gov

Sublingual Misoprostol Versus Standard Surgical Care for the Treatment of Incomplete Abortion

NACompletedINTERVENTIONAL
Enrollment

1,000

Participants

Timeline

Start Date

February 28, 2007

Primary Completion Date

November 30, 2009

Study Completion Date

November 30, 2009

Conditions
Incomplete Abortion
Interventions
DRUG

misoprostol

single dose of 400 mcg misoprostol administered sublingually

PROCEDURE

surgery

standard surgical treatment (dilation and curettage or manual vacuum aspiration)

Trial Locations (6)

Unknown

Dandé District Hospital/Ziniaré District Hospital, Dande/Ziniare

El-Galaa Teaching Hospital, Cairo

Shatby Maternity Hospital/Alexandria University, Shatby, Alexandria

Cheikh Zayed Hospital, Nouakchott

Maternite Issaka Gazobi, Niamey

Centre de Sante Le Roi Baudouin, Guédiawaye

All Listed Sponsors
lead

Gynuity Health Projects

OTHER

NCT00466999 - Sublingual Misoprostol Versus Standard Surgical Care for the Treatment of Incomplete Abortion | Biotech Hunter | Biotech Hunter