Study of 400mcg Sublingual Versus 400mcg Buccal Misoprostol Following 200mg Mifepristone for Medical Abortion up to 63 Days Last Menstrual Period (LMP)
Clinical trial NCT00870272 · COMPLETED
Trial details
- NCT number
- NCT00870272
- Sponsor
- Gynuity Health Projects
- Status
- COMPLETED
- Phase
- Not Applicable
- Study type
- INTERVENTIONAL
- Start date
- 2007-07-01
- Primary completion
- 2009-03-01
- Enrollment
- 550
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