Clinical trial
Study to Evaluate the Safety and Efficacy of Seasonale for Treatment of Low Bone…
NCT00117260 · Duramed Research, Industry · Withdrawn
Key facts
| NCT number | NCT00117260 |
|---|---|
| Title | Study to Evaluate the Safety and Efficacy of Seasonale for Treatment of Low Bone Mineral Density |
| Official title | A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of a 91-Day Extended-Cycle Combination Oral Contraceptive (Seasonale) for the Treatment of Low Bone Mineral Density in Adolescent Females With Secondary Amenorrhea and Osteopenia |
| Lead sponsor | Duramed Research, Industry |
| Status | Withdrawn |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Osteopenia |
| Intervention type | Drug |
| Interventions | Seasonale (levonorgestrel and ethinyl estradiol) |
| Enrollment | 0 |
| Start date | Jul 1, 2005 |
| Primary completion | Jul 1, 2007 |
| Completion | Aug 1, 2007 |
| First posted | Jul 6, 2005 |
| Last update posted | Aug 12, 2013 |
At a glance
- 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: