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Clinical trial

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

NCT00286208 is registered in ClinicalTrials.gov with Gynuity Health Projects as lead sponsor.

NCT NCT00286208
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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized Study of Sublingual Versus Oral Misoprostol Administration Following Mifepristone 200 mg for Abortion up to 63 Days Gestation
Lead sponsor
Gynuity Health Projects
Phase
Not applicable
Overall status
Completed
Start date
August 31, 2005
Completion date
January 31, 2008
Enrollment
1,443 (actual)
Sites
9

Conditions

As the registry lists them; a condition with its own page is linked.

induced abortion