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Clinical trial

Study of 400mcg Versus 800mcg Buccal Misoprostol Following Mifepristone 200mg for Abortion up to 63 Days Gestation

NCT00482209 is registered in ClinicalTrials.gov with Gynuity Health Projects as lead sponsor.

NCT NCT00482209
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Registry record

As filed in ClinicalTrials.gov.

Title
Study of 400mcg Versus 800mcg Buccal Misoprostol Following Mifepristone 200mg for Abortion up to 63 Days Gestation
Lead sponsor
Gynuity Health Projects
Phase
Not applicable
Overall status
Completed
Start date
May 31, 2007
Completion date
October 31, 2009
Enrollment
1,220 (estimated)
Sites
4

Conditions

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

induced abortion