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Completed Phase 3 Interventional Results available

DHEA Against Vaginal Atrophy - Safety Study of 12 Months

ClinicalTrials.gov ID: NCT01256671

Public ClinicalTrials.gov record NCT01256671. 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 Jul 21, 2026, 6:52 PM EDT

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

Study identification

NCT ID
NCT01256671
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
EndoCeutics Inc.
Industry
Enrollment
530 participants

Conditions and interventions

Interventions

  • DHEA Drug

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
Nov 30, 2010
Primary completion
Jun 30, 2012
Completion
Nov 30, 2012
Last update posted
Oct 17, 2017

2010 – 2012

United States locations

U.S. sites
31
U.S. states
20
U.S. cities
29
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 # 07 Washington D.C. District of Columbia 20036
EndoCeutics site # 45 Boynton Beach Florida 33472
EndoCeutics site # 26 Jacksonville Florida 32207
EndoCeutics site # 41 West Palm Beach Florida 33401
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 # 24 Omaha Nebraska 68131
EndoCeutics site # 28 Moorestown New Jersey 08057
EndoCeutics site # 50 Neptune City New Jersey 07753
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 # 33 Beachwood Ohio 44122
EndoCeutics site # 05 Cleveland Ohio 44122
EndoCeutics site # 47 Cleveland Ohio 44124
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
EndoCeutics site # 38 Renton Washington 98055

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 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01256671, 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 Oct 17, 2017 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01256671 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →