Clinical trial
Study of 400mcg Versus 800mcg Buccal Misoprostol Following Mifepristone 200mg…
NCT00482209 · Gynuity Health Projects, Other · Completed
Key facts
| NCT number | NCT00482209 |
|---|---|
| Title | Study of 400mcg Versus 800mcg Buccal Misoprostol Following Mifepristone 200mg for Abortion up to 63 Days Gestation |
| Lead sponsor | Gynuity Health Projects, Other |
| Status | Completed |
| Study type | Interventional |
| Conditions | Induced Abortion |
| Intervention type | Drug |
| Interventions | Mifepristone, misoprostol, mifepristone |
| Enrollment | 1,220 |
| Start date | May 1, 2007 |
| Primary completion | Oct 1, 2009 |
| Completion | Oct 1, 2009 |
| First posted | Jun 5, 2007 |
| Last update posted | Oct 12, 2009 |
| Countries | Georgia, Vietnam |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: