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Study Evaluating Bazedoxifene/Conjugated Estrogen Combinations in Vasomotor Symptoms Associated With Menopause
NCT00238732 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to determine whether Bazedoxifine/conjugated estrogens are effective in the treatment of vaginal atrophy.
Conditions Studied
Interventions
- DRUG Bazedoxifene/Conjugated Estrogen
Study Locations (20)
Florida
- — Aventura
- — Gainesville
- — Miami
- — Palm Harbor
- — Palm Springs
- — Pinnellas Park
- — Stuart
- — Tampa
- — West Palm Beach
California
- — Oakland
- — San Diego
- — Upland
Connecticut
- — Avon
- — Groton
- — Waterbury
Alabama
- — Birmingham
- — Montgomery
Arizona
- — Scottsdale
- — Tucson
Colorado
- — Denver
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 650 participants |
| Start Date | 2005-10 |
| Est. Completion | 2007-03 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00238732
The ClinicalTrials.gov registry entry for NCT00238732 describes a study currently listed as completed. It is categorized as Phase 3, 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 650 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wyeth is now a wholly owned subsidiary of Pfizer, which has 31 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 Vaginal Atrophy appearing as the primary indexed condition, and to 1 intervention — of which Bazedoxifene/Conjugated Estrogen 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: NCT00238732 reports 20 study locations spanning 6 distinct geographic areas — top geographies include Florida, California, Connecticut. 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 NCT00238732 about?
NCT00238732 is a clinical study titled "Study Evaluating Bazedoxifene/Conjugated Estrogen Combinations in Vasomotor Symptoms Associated With Menopause". The purpose of this study is to determine whether Bazedoxifine/conjugated estrogens are effective in the treatment of vaginal atrophy.
What is the current status of trial NCT00238732?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 650 participants. The study started on 2005-10. Estimated completion is 2007-03.
What conditions does trial NCT00238732 study?
This clinical trial studies the following conditions: Vaginal Atrophy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00238732?
The interventions under investigation include: Bazedoxifene/Conjugated Estrogen (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00238732?
This trial is sponsored by Wyeth is now a wholly owned subsidiary of Pfizer, which has 31 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00238732 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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