Mifepristone, misoprostol
Sponsors
Gynuity Health Projects, University of Pittsburgh
Conditions
Abortion, InducedComplete AbortionInduced Abortion
Phase 2
Unknown Phase
Study of Sublingual Versus Oral Misoprostol Administration Following Mifepristone 200 mg for Abortion up to 63 Days Gestation
CompletedNCT00286208
Start: 2005-08-31End: 2008-01-31Updated: 2014-02-19
Study of 400mcg Versus 800mcg Buccal Misoprostol Following Mifepristone 200mg for Abortion up to 63 Days Gestation
CompletedNCT00482209
Start: 2007-05-31End: 2009-10-31Target: 1220Updated: 2009-10-12
Study of 400mcg Versus 800mcg Buccal Misoprostol Following Mifepristone 200mg for Abortion up to 63 Days Gestation
CompletedNCT00482209
Start: 2007-05-31End: 2009-10-31Target: 1220Updated: 2009-10-12
Expansion Study of a Simplified Regimen of Medical Abortion Thru 63 Last Menstrual Period (LMP) in Tunisia
CompletedNCT01173003
Start: 2009-06-30End: 2011-12-31Updated: 2014-02-19
Mifepristone and Misoprostol for the Termination of Pregnancy up to 70 Days' Gestation in Kazakhstan
CompletedNCT02018796
Start: 2013-10-31End: 2014-12-31Updated: 2015-08-13