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Completed Phase 3 Interventional Results available

DHEA Against Vaginal Atrophy - 3-Month Efficacy Study

ClinicalTrials.gov ID: NCT01256684

Public ClinicalTrials.gov record NCT01256684. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 4:20 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this Phase III trial is to confirm the efficacy of intravaginal dehydroepiandrosterone (DHEA) in postmenopausal women with vaginal atrophy.

Study identification

NCT ID
NCT01256684
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
EndoCeutics Inc.
Industry
Enrollment
255 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
40 Years to 75 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2010 (Type not available)
Primary completion
Aug 2011 (Actual)
Completion
Nov 2011 (Actual)
Last update posted
Jun 26, 2017

2010 – 2011

United States locations

U.S. sites
24
U.S. states
18
U.S. cities
23
Facility City State ZIP Site status
EndoCeutics site # 39 Montgomery Alabama 36117 —
EndoCeutics site # 14 Tucson Arizona 85712 —
EndoCeutics site # 21 Sacramento California 95821 —
EndoCeutics site # 30 San Diego California 92108 —
EndoCeutics site # 17 San Diego California 92120 —
EndoCeutics site # 36 Denver Colorado 80218 —
EndoCeutics site # 42 Milford Connecticut 06460 —
EndoCeutics site # 45 Boynton Beach Florida 33472 —
EndoCeutics site # 26 Jacksonville Florida 32207 —
EndoCeutics site # 23 Sandy Springs Georgia 30328 —
EndoCeutics site # 10 Meridian Idaho 83642 —
EndoCeutics site # 27 Baltimore Maryland 21285-6815 —
EndoCeutics site # 22 Kalamazoo Michigan 49009 —
EndoCeutics site # 25 Lincoln Nebraska 68510 —
EndoCeutics site # 28 Moorestown New Jersey 08057 —
EndoCeutics site # 44 New Brunswick New Jersey 08901 —
EndoCeutics site # 19 New York New York 10016 —
EndoCeutics site # 16 Durham North Carolina 27713 —
EndoCeutics site # 05 Cleveland Ohio 44122 —
EndoCeutics site # 15 Columbus Ohio 43213 —
EndoCeutics site # 35 Pittsburgh Pennsylvania 15206 —
EndoCeutics site # 09 West Jordan Utah 84088 —
EndoCeutics site # 31 Charlottesville Virginia 22903 —
EndoCeutics site # 03 Norfolk Virginia 23507 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01256684, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 26, 2017 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01256684 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →