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Completed Phase 3 Interventional Results available

Intravaginal Prasterone (DHEA) Against Vulvovaginal Atrophy Associated With Menopause

ClinicalTrials.gov ID: NCT02013544

Public ClinicalTrials.gov record NCT02013544. 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, 4:51 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
NCT02013544
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
EndoCeutics Inc.
Industry
Enrollment
558 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • Prasterone (DHEA) Drug

Drug

Eligibility (public fields only)

Age range
40 Years to 80 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
Jan 31, 2014
Primary completion
Dec 31, 2014
Completion
Jan 31, 2015
Last update posted
May 31, 2017

2014 – 2015

United States locations

U.S. sites
24
U.S. states
15
U.S. cities
22
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 # 83 San Diego California 92103
EndoCeutics site # 30 San Diego California 92108
EndoCeutics site # 36 Denver Colorado 80209
EndoCeutics site # 52 Denver Colorado 80220
EndoCeutics site # 45 Boynton Beach Florida 33472
EndoCeutics site # 60 Lake Worth Florida 33461
EndoCeutics site # 54 North Miami Florida 33161
EndoCeutics site # 80 West Palm Beach Florida 33409
EndoCeutics site # 23 Atlanta Georgia 30328
EndoCeutics site # 55 Wichita Kansas 67226
EndoCeutics site # 86 Louisville Kentucky 40291
EndoCeutics site # 27 Lutherville Maryland 21093
EndoCeutics site # 87 Lawrenceville New Jersey 08648
EndoCeutics site # 81 Plainsboro New Jersey 08536
EndoCeutics site # 05 Cleveland Ohio 44122
EndoCeutics site # 15 Columbus Ohio 43213
EndoCeutics site # 75 Philadelphia Pennsylvania 19114-1029
EndoCeutics site # 84 Corpus Christi Texas 78414
EndoCeutics site # 82 Houston Texas 77030
EndoCeutics site # 03 Norfolk Virginia 23507
EndoCeutics site # 76 Seattle Washington 98105

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 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02013544, 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 May 31, 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 NCT02013544 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →