Study of 400mcg Versus 800mcg Buccal Misoprostol Following Mifepristone 200mg for Abortion up to 63 Days Gestation
Clinical trial NCT00482209 · COMPLETED
Trial details
- NCT number
- NCT00482209
- Sponsor
- Gynuity Health Projects
- Status
- COMPLETED
- Phase
- Not Applicable
- Study type
- INTERVENTIONAL
- Start date
- 2007-05-01
- Primary completion
- 2009-10-01
- Enrollment
- 1220
Track trials programmatically
Sponsors, conditions and status changes through the Atlas API.