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Study of the Efficacy of ESTRATEST® H.S. Tablets in Relieving Menopausal Symptoms in Estrogenized Postmenopausal Women
NCT00141570 · View on ClinicalTrials.gov ↗
Study Summary
To determine whether treatment with ESTRATEST® H.S. Tablets is superior to treatment with esterified estrogens tablets
Conditions Studied
Interventions
- DRUG esterified estrogens 0.625 mg and methyltestosterone 1.25 mg
Study Locations (20)
California
- Site 68 — Carmichael
- Site 55 — Encinitas
- Site 6 — San Diego
- Site 45 — Santa Rosa
- Site 25 — Walnut Creek
Connecticut
- Site 1 — Groton
- Site 54 — Hartford
- Site 30 — Trumbull
- Site 34 — Waterbury
Alabama
- Site 66 — Huntsville
- Site 57 — Mobile
- Site 46 — Montgomery
Florida
- Site 10 — Aventura
- Site 73 — Fort Myers
- Site 51 — Leesburg
Arizona
- Site 29 — Phoenix
- Site 15 — Tucson
Arkansas
- Site 3 — Jonesboro
- Site 22 — Little Rock
Colorado
- Site 26 — Denver
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 350 participants |
| Start Date | 2004-06 |
| Est. Completion | 2007-06 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00141570
The ClinicalTrials.gov registry entry for NCT00141570 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 350 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Solvay Pharmaceuticals, which has 5 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Menopause appearing as the primary indexed condition, and to 1 intervention — of which esterified estrogens 0.625 mg and methyltestosterone 1.25 mg is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00141570 reports 20 study locations spanning 7 distinct geographic areas — top geographies include California, Connecticut, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00141570 about?
NCT00141570 is a clinical study titled "Study of the Efficacy of ESTRATEST® H.S. Tablets in Relieving Menopausal Symptoms in Estrogenized Postmenopausal Women". To determine whether treatment with ESTRATEST® H.S. Tablets is superior to treatment with esterified estrogens tablets
What is the current status of trial NCT00141570?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 350 participants. The study started on 2004-06. Estimated completion is 2007-06.
What conditions does trial NCT00141570 study?
This clinical trial studies the following conditions: Menopause. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00141570?
The interventions under investigation include: esterified estrogens 0.625 mg and methyltestosterone 1.25 mg (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00141570?
This trial is sponsored by Solvay Pharmaceuticals, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00141570 being conducted?
This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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