Actively Recruiting

All Genders
ID02448485

High-Sensitivity Troponin T Plasma Levels in Patients With Aortic Stenosis

Led by Medical University Innsbruck · Updated on 2024-08-01

10000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the clinical importance of slightly raised high-sensitivity troponin T (hs-TnT) levels in people with both asymptomatic and symptomatic aortic stenosis. This condition can lead to serious heart symptoms like heart failure, fainting, or chest pain, which often guide the decision for valve surgery. The study aims to improve risk assessment beyond current methods, which can be subjective or limited by technical challenges and patient factors like low blood flow or heart valve calcification. The study observes two groups: patients who have had an aortic valve intervention, either surgical or transcatheter, and those with aortic stenosis managed without surgery. Researchers use routine blood tests measuring hs-TnT to evaluate ongoing heart muscle damage or fibrosis. They also consider other clinical evaluations like echocardiography and computed tomography, but focus on hs-TnT as a potentially objective and accessible marker of disease severity. Participants are followed over time to track outcomes including overall and cardiovascular mortality for up to eight years. The study involves regular clinical assessments and blood testing to monitor heart status. By examining these measurements, the research team hopes to better predict disease progression and outcomes for people with aortic stenosis, helping to guide treatment decisions and improve care.

CONDITIONS

Brief Title

High-Sensitivity Troponin T Plasma Levels in Patients With Aortic Stenosis (Tyrolean Aortic Stenosis Study-2)

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aortic stenosis confirmed by echocardiography or invasive tests
Not Eligible

You will not qualify if you...

  • Acute coronary syndrome
  • Endocarditis

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Varies depending on initial assessment schedule

Participants undergo assessments including echocardiography and other tests to confirm aortic stenosis and evaluate heart function.

1 to 2 visits depending on clinical condition

Long-term Monitoring

Duration - Up to 8 years

Participants with aortic stenosis are observed over time to monitor disease progression and outcomes, with some undergoing aortic valve intervention while others are followed conservatively.

Follow-up visits scheduled according to clinical needs

Trial Site Locations

Total: 1 location

1

Medical University Innsbruck

Innsbruck, Tyrol, Austria, 6020

Actively Recruiting

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Research Team

W

Wolfgang Dichtl, MD, PhD

F

Fabian Barbieri

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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