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DHEA Against Vaginal Atrophy - 3-Month Efficacy Study

Vaginal Atrophy Clinical Trial

Official title:
DHEA Against Vaginal Atrophy (Placebo-controlled, Double-blind and Randomized Phase III Study of 3-month Intravaginal DHEA)

Clinical Trial Summary

The purpose of this Phase III trial is to confirm the efficacy of intravaginal dehydroepiandrosterone (DHEA) in postmenopausal women with 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 NCT01256684
Study type Interventional
Source EndoCeutics Inc.
Contact
Status Completed
Phase Phase 3
Start date December 2010
Completion date November 2011
View Details
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