Clinical trial
Effect of Intravaginal Prasterone (DHEA) on Moderate to Severe Symptoms of Vulvovaginal Atrophy Due to Menopause, in Women Under Treatment With an Aromatase Inhibitor for Breast Cancer - (Placebo-Controlled, Double Blind and Randomized Phase III Study)
NCT03740945 is registered in ClinicalTrials.gov with EndoCeutics Inc. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Effect of Intravaginal Prasterone (DHEA) on Moderate to Severe Symptoms of Vulvovaginal Atrophy Due to Menopause, in Women Under Treatment With an Aromatase Inhibitor for Breast Cancer - (Placebo-Controlled, Double Blind and Randomized Phase III Study)
- Lead sponsor
- EndoCeutics Inc.
- Phase
- Phase 3
- Overall status
- Withdrawn
- Start date
- November 6, 2018
- Completion date
- December 5, 2019
- Enrollment
- 0 (actual)
- Sites
- Not reported
Conditions
As the registry lists them; a condition with its own page is linked.
vaginal atrophy in breast cancer patients