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Terminated Phase 2 Interventional

The Efficacy of ESTRATEST® Tablets in Relieving Menopausal Symptoms in Estrogenized, Hysterectomized Postmenopausal Women

ClinicalTrials.gov ID: NCT00141557

Public ClinicalTrials.gov record NCT00141557. 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 May 6, 2026, 12:51 AM EDT

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

Official title

A Multi-Center, Double-Blind Study to Determine the Efficacy of ESTRATEST® Tablets in Relieving Menopausal Symptoms in Estrogenized, Hysterectomized Postmenopausal Women

Study identification

NCT ID
NCT00141557
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Solvay Pharmaceuticals
Industry
Enrollment
133 participants

Conditions and interventions

Conditions

Interventions

  • Esterified estrogens 1.25 mg Drug
  • esterified estrogens 1.25mg and methyltestosterone 2.5mg Drug

Drug

Eligibility (public fields only)

Age range
35 Years to 65 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
Jun 30, 2004
Primary completion
Mar 31, 2007
Completion
Feb 29, 2008
Last update posted
Apr 10, 2008

2004 – 2008

United States locations

U.S. sites
78
U.S. states
29
U.S. cities
78
Facility City State ZIP Site status
Site 66 Huntsville Alabama
Site 57 Mobile Alabama
Site 46 Montgomery Alabama
Site 29 Phoenix Arizona
Site 15 Tucson Arizona
Site 3 Jonesboro Arkansas
Site 22 Little Rock Arkansas
Site 68 Carmichael California
Site 55 Encinitas California
Site 6 San Diego California
Site 45 Santa Rosa California
Site 25 Walnut Creek California
Site 26 Denver Colorado
Site 1 Groton Connecticut
Site 54 Hartford Connecticut
Site 30 Trumbull Connecticut
Site 34 Waterbury Connecticut
Site 10 Aventura Florida
Site 78 Clearwater Florida
Site 73 Fort Myers Florida
Site 51 Leesburg Florida
Site 49 Melbourne Florida
Site 64 New Port Richey Florida
Site 61 Ocala Florida
Site 27 Palm Springs Florida
Site 11 Pinellas Park Florida
Site 75 Sarasota Florida
Site 69 St. Petersburg Florida
Site 70 Venice Florida
Site 17 West Palm Beach Florida
Site 50 Alpharetta Georgia
Site 5 Atlanta Georgia
Site 44 Decatur Georgia
Site 77 Douglasville Georgia
Site 9 Riverdale Georgia
Site 7 Savannah Georgia
Site 47 Boise Idaho
Site 24 Champaign Illinois
Site 20 Chicago Illinois
Site 76 Peoria Illinois
Site 58 Evansville Indiana
Site 39 Wichita Kansas
Site 59 Baton Rouge Louisiana
Site 52 New Orleans Louisiana
Site 53 Ann Arbor Michigan
Site 63 Kansas City Missouri
Site 32 Richmond Heights Missouri
Site 36 St Louis Missouri
Site 72 Billings Montana
Site 21 Lincoln Nebraska
Site 37 Reno Nevada
Site 65 Cary North Carolina
Site 13 New Bern North Carolina
Site 16 Winston-Salem North Carolina
Site 60 Columbus Ohio
Site 67 Oklahoma City Oklahoma
Site 40 Tulsa Oklahoma
Site 62 Eugene Oregon
Site 41 Medford Oregon
Site 33 Portland Oregon
Site 18 Erie Pennsylvania
Site 19 Philadelphia Pennsylvania
Site 23 Pottstown Pennsylvania
Site 31 Anderson South Carolina
Site 35 Greer South Carolina
Site 4 Chattanooga Tennessee
Site 74 Conroe Texas
Site 8 Corpus Christi Texas
Site 71 Dallas Texas
Site 42 Houston Texas
Site 14 San Antonio Texas
Site 38 Salt Lake City Utah
Site 28 Norfolk Virginia
Site 12 Richmond Virginia
Site 56 Renton Washington
Site 2 Seattle Washington
Site 48 Spokane Washington
Site 43 Tacoma Washington

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00141557, 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 Apr 10, 2008 · Synced May 6, 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 NCT00141557 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →