Clinical trial
Efficacy and Long-Term Safety of Ospemifene in the Treatment of Vulvar and Vaginal Atrophy (VVA) in Postmenopausal Women: A 52-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study Comparing 60 MG Oral Daily Dose of Ospemifene With Placebo
NCT00566982 is registered in ClinicalTrials.gov with Shionogi as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Efficacy and Long-Term Safety of Ospemifene in the Treatment of Vulvar and Vaginal Atrophy (VVA) in Postmenopausal Women: A 52-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study Comparing 60 MG Oral Daily Dose of Ospemifene With Placebo
- Lead sponsor
- Shionogi
- Phase
- Phase 3
- Overall status
- Completed
- Start date
- October 31, 2007
- Completion date
- July 31, 2009
- Enrollment
- 426 (actual)
- Sites
- Not reported
Conditions
As the registry lists them; a condition with its own page is linked.