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Recruiting NCT06595407

Loss of Y Chromosome in Aortic Stenosis

Observational Aortic Stenosis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Blood analysis for loss-of-Y chromosome.
Who it may be relevant to
Registry conditions: Aortic Stenosis. Basic parameters: from 40 years · Male.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The most common heart valve disease in humans is aortic stenosis which is a critical narrowing of the valve through which the heart has to pump blood to the rest of the body. This condition occurs in 2-3% of adults over 65 years of age and when it progresses to a severe stage leads to heart failure and need for valve replacement procedures (including surgery and catheter-based replacement). Aortic stenosis has a strong male predominance. The purpose of this study is to evaluate whether loss of Y-chromosome from circulating blood cells in males, which has been associated with TGF-beta-related fibrosis of other organs, is associated with the development of aortic stenosis.

Interventions

  • Diagnostic test Blood analysis for loss-of-Y chromosome
    Analysis for the percentage of circulating leukocytes with loss-of-y chromosome

Primary outcome measures

  • Loss of Y chromosome [Time frame: 1 day]

Eligibility criteria

Inclusion criteria

  • Aortic stenosis (valve area \<1.5cm2)

Exclusion criteria

  • Bicuspid aortic valve
  • History of radiation to chest
  • Inflammatory (autoimmune, rheumatologic) disease associated with aortic stenosis
  • Active cancer

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-control

Study locations

United States · 1 center
  • University of Virginia — Charlottesville

Identifiers

NCT: NCT06595407 · 301597

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗