drugset / Trial / NCT01846442

Topical DHEA Against Vaginal Atrophy

NCT01846442 ↗

Phase 3 Completed 218 enrolled EndoCeutics Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine the dose-response of vaginal mucosa parameters to the local action of DHEA (Dehydroepiandrosterone) in postmenopausal women suffering from vaginal atrophy.

Timeline

Start
2007-06
Primary completion
2008-05
Completion
2008-10

Outcome

Met primary endpoint

paper At the standard 12-week time interval, 0.5% DHEA caused a 45.9 +/- 5.31 (P < 0.0001 vs placebo) decrease in the percentage of parabasal cells PMID 19436225 ↗

paper a 6.8 +/- 1.29% (P < 0.0001) increase in superficial cells, a 1.3 +/- 0.13 unit (P < 0.0001) decrease in vaginal pH PMID 19436225 ↗

paper and a 1.5 +/- 0.14 score unit (P < 0.0001) decrease in the severity of the most bothersome symptom. PMID 19436225 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject DHEA Unknown 3.25 mg Other
Subject DHEA Unknown 6.5 mg Other
Subject DHEA Unknown 13 mg Other