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Study of Sublingual Versus Oral Misoprostol Administration Following Mifepristone 200 mg for Abortion up to 63 Days Gestation

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT00286208
Recruitment Status : Completed
First Posted : February 3, 2006
Last Update Posted : February 19, 2014
Sponsor:
Information provided by (Responsible Party):
Gynuity Health Projects

No Study Results Posted on ClinicalTrials.gov for this Study
Recruitment Status : Completed
Actual Primary Completion Date : January 2008
Actual Study Completion Date : January 2008