Clinical trial
Study of Sublingual Versus Oral Misoprostol Administration Following…
NCT00286208 · Gynuity Health Projects, Other · Completed
Key facts
| NCT number | NCT00286208 |
|---|---|
| Title | Study of Sublingual Versus Oral Misoprostol Administration Following Mifepristone 200 mg for Abortion up to 63 Days Gestation |
| Official title | A Randomized Study of Sublingual Versus Oral Misoprostol Administration Following Mifepristone 200 mg 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 |
| Enrollment | 1,443 |
| Start date | Aug 1, 2005 |
| Primary completion | Jan 1, 2008 |
| Completion | Jan 1, 2008 |
| First posted | Feb 3, 2006 |
| Last update posted | Feb 19, 2014 |
| Countries | Moldova, Tunisia, Turkey (Türkiye) |
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: