Multicenter, Randomized, Open Label, Parallel-Group Study to Evaluate User Satisfaction, Acceptability, and Tolerability of the Ultra Low Dose Levonorgestrel Intrauterine Contraceptive System with 12u01/15/2011 - 12/31/2015 (PI)
Bayer Schering Pharma AG (Germany)
Multi-center, Open-label, Randomized Study to Assess the Safety and Contraceptive Efficacy of Two Doses (In Vitro 12pg/24 h) of the Ultra Low Dose Levonorges12/01/2007 - 12/31/2013 (PI)
Bayer AG
Multicenter, open-label, uncontrolled study to investigate the efficacy and safety of the transdermal contraceptive patch containing 0.55 mg ethinyl estradiol and 2.1 mg gestodene (material no. 805/01/2009 - 12/31/2011 (PI)
Bayer AG
Mifepristone vs Misoprostol for Cervical Preparation Prior to Surgical Abortion between 11 & 15 week06/01/2012 - 06/30/2015 (PI)
Society of Family Planning
Mifepristone vs. Osmotic Dilator Insertion for Cervical Preparation Prior to Surgical Abortion07/01/2011 - 09/30/2014 (PI)
Society of Family Planning
Cervical preparation before dilation and evacuation at 16-24 weeks gestation: A multicenter randomiz03/22/2013 - 12/31/2013 (PI)
Society of Family Planning
Mifepristone versus laminaria for cervical preparation prior to surgical abortion at 14-16 weeks10/01/2009 - 10/01/2011 (PI)
Society of Family Planning
Misoprostol for treatment of fetal death at 14-18 weeks of pregnancy, inclusive, not accompanied by11/01/2008 - 10/31/2009 (PI)
Gynuity Health Projects, LLC