Clinical trial
A Study to Evaluate the Efficacy of Seasonique for the Treatment of Cyclic…
NCT00196365 · Duramed Research, Industry · Completed
Key facts
| NCT number | NCT00196365 |
|---|---|
| Title | A Study to Evaluate the Efficacy of Seasonique for the Treatment of Cyclic Pelvic Pain |
| Official title | A Study to Compare the Efficacy of an Extended-cycle Oral Contraceptive, Seasonique Which Utilizes Ethinyl Estradiol During the Usual Hormone-free Interval Compared to Conventional Oral Contraceptive Therapy for Cyclic Pelvic Pain |
| Lead sponsor | Duramed Research, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Dysmenorrhea |
| Intervention type | Drug |
| Interventions | levonorgestrel/EE 0.15/0.03 and EE 0.01 mg tablets, levonorgestrel/EE 0.15/0.03 mg tablets and placebo |
| Enrollment | 97 |
| Start date | Jan 1, 2005 |
| Primary completion | Jul 1, 2007 |
| Completion | Jul 1, 2007 |
| First posted | Sep 20, 2005 |
| Last update posted | May 12, 2014 |
| Countries | United States |
At a glance
- 10–99 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: