Clinical trial
A Study to Evaluate Bleeding Patterns With Three Different Doses of DR-1031…
NCT00394771 · Duramed Research, Industry · Completed
Key facts
| NCT number | NCT00394771 |
|---|---|
| Title | A Study to Evaluate Bleeding Patterns With Three Different Doses of DR-1031 Compared to Seasonale |
| Official title | A Prospective, Multicenter, Double-Blinded, Randomized Study to Evaluate Bleeding Patterns in Women Using One of Three Different Doses of DR-1031 Oral Contraceptive Compared to Seasonale Oral Contraceptive Regimen |
| Lead sponsor | Duramed Research, Industry |
| Status | Completed |
| Phase | Phase 2 |
| Study type | Interventional |
| Conditions | Breakthrough Bleeding |
| Intervention type | Drug |
| Interventions | DR-1031, Seasonale®, Portia® |
| Enrollment | 567 |
| Start date | Oct 1, 2006 |
| Primary completion | Mar 1, 2008 |
| Completion | Mar 1, 2008 |
| First posted | Nov 1, 2006 |
| Last update posted | Jul 26, 2013 |
| Countries | United States |
At a glance
- 10–99 Study sites
- Yes 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: