Clinical trial
Efficacy and Safety of Oral DHEA Therapy for Postmenopausal Women on Sexual…
NCT00289926 · Monash University, Other · Completed
Key facts
| NCT number | NCT00289926 |
|---|---|
| Title | Efficacy and Safety of Oral DHEA Therapy for Postmenopausal Women on Sexual Function, Wellbeing and Vasomotor Symptoms |
| Official title | A Randomised, Double-blind, Placebo-controlled, Parallel-group, 52-week Study to Evaluate the Efficacy and Safety of Oral DHEA Therapy for Postmenopausal Women on Sexual Function, Wellbeing and Vasomotor Symptoms |
| Lead sponsor | Monash University, Other |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Quality of Life, Menopausal Syndrome, Libido Disorder |
| Intervention type | Drug |
| Interventions | dehydroepiandrosterone, placebo |
| Enrollment | 240 |
| Start date | Feb 1, 2006 |
| Primary completion | Apr 1, 2008 |
| Completion | Apr 1, 2008 |
| First posted | Feb 10, 2006 |
| Last update posted | Mar 16, 2016 |
| Countries | Australia |
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: