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Completed Phase 3 Interventional Results available

Dehydroepiandrosterone (DHEA) Against Vaginal Atrophy

ClinicalTrials.gov ID: NCT01358760

Public ClinicalTrials.gov record NCT01358760. 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
NCT01358760
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
EndoCeutics Inc.
Industry
Enrollment
450 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • 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
May 31, 2011
Primary completion
Mar 31, 2012
Completion
Apr 30, 2012
Last update posted
Jun 11, 2017

2011 – 2012

United States locations

U.S. sites
32
U.S. states
20
U.S. cities
30
Facility City State ZIP Site status
EndoCeutics site # 39 Montgomery Alabama 36117
EndoCeutics site # 14 Tucson Arizona 85712
EndoCeutics site # 65 Little Rock Arkansas 72204
EndoCeutics site # 21 Sacramento California 95821
EndoCeutics site # 30 San Diego California 92108
EndoCeutics site # 36 Denver Colorado 80218
EndoCeutics site # 52 Denver Colorado 80220
EndoCeutics site # 66 Danbury Connecticut 06810
EndoCeutics site # 42 Milford Connecticut 06460
EndoCeutics site # 57 West Hartford Connecticut 06117
EndoCeutics site # 61 Newark Delaware 19718
EndoCeutics site # 26 Jacksonville Florida 32207
EndoCeutics site # 60 Lake Worth Florida 33461
EndoCeutics site # 54 North Miami Florida 33161
EndoCeutics site # 56 Pinellas Park Florida 33781
EndoCeutics site # 23 Sandy Springs Georgia 30328
EndoCeutics site # 10 Meridian Idaho 83642
EndoCeutics site # 55 Wichita Kansas 67226
EndoCeutics site # 27 Baltimore Maryland 21285-6815
EndoCeutics site # 24 Omaha Nebraska 68131
EndoCeutics site # 50 Neptune City New Jersey 07753
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 # 62 Providence Rhode Island 02930
EndoCeutics site # 64 Jackson Tennessee 38305
EndoCeutics site # 63 Memphis Tennessee 38120
EndoCeutics site # 53 San Antonio Texas 78205
EndoCeutics site # 51 Sandy City Utah 84070
EndoCeutics site # 09 West Jordan Utah 84088
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 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01358760, 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 11, 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 NCT01358760 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →