Clinical trial
A Randomized Trial of Buccal Compared to Oral Misoprostol Following Mifepristone…
NCT00386867 · Gynuity Health Projects, Other · Completed
Key facts
| NCT number | NCT00386867 |
|---|---|
| Title | A Randomized Trial of Buccal Compared to Oral Misoprostol Following Mifepristone for Medical Abortion up to 63 Days LMP |
| Lead sponsor | Gynuity Health Projects, Other |
| Status | Completed |
| Study type | Interventional |
| Conditions | Abortion, Induced |
| Intervention type | Drug |
| Interventions | 800 mcg misoprostol via oral or buccal administration |
| Enrollment | 1,200 |
| Start date | Oct 1, 2006 |
| Completion | Mar 1, 2007 |
| First posted | Oct 12, 2006 |
| Last update posted | Jun 5, 2007 |
| Countries | United States |
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: