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Topical DHEA Against Vaginal Atrophy

Vaginal Atrophy Clinical Trial

Official title:
Topical DHEA Against Vaginal Atrophy (3-Month Placebo-Controlled Double-Blind Randomized Phase III Study)

Clinical Trial Summary

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

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01846442
Study type Interventional
Source EndoCeutics Inc.
Contact
Status Completed
Phase Phase 3
Start date June 2007
Completion date October 2008
View Details
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