Actively Recruiting

Age: 18Years +
All Genders
ID07382128

Myocardial Perfusion CMR for Differentiating and Characterizing Hypertrophic Cardiomyopathy Phenotypes

Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2026-02-02

250

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating myocardial perfusion abnormalities using cardiac magnetic resonance (CMR) perfusion imaging in patients with hypertrophic cardiomyopathy (HCM) types, including sarcomeric and non-sarcomeric HCM, Anderson-Fabry disease, and cardiac amyloidosis. The study also includes first-degree relatives of affected patients and genetic mutation carriers. By comparing blood flow and perfusion patterns, the study aims to identify distinctive signs that may improve diagnosis, risk assessment, and understanding of ischemia's role in disease progression and outcomes. This observational study involves imaging participants' hearts with CMR to assess myocardial perfusion. Participants include those diagnosed with hypertrophic cardiomyopathy or related genetic conditions, their close relatives, and genetic mutation carriers. The study will analyze quantitative and qualitative perfusion defects at the start and again after 36 months to observe changes over time. Participants will undergo cardiac magnetic resonance imaging at baseline and after 36 months. Researchers will measure and compare perfusion defects using both quantitative and qualitative methods. The study focuses on gathering detailed imaging data to understand myocardial blood flow differences among the various cardiomyopathy types and genetic profiles. The total participation time involves these two main imaging timepoints, with ongoing observation to support long-term insights.

CONDITIONS

Brief Title

Myocardial Perfusion CMR for Differentiating and Characterizing Hypertrophic Cardiomyopathy Phenotypes

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of hypertrophic cardiomyopathy or related phenotype according to current ESC guidelines, or first-degree relative of such a patient, or genetic mutation carrier for hypertrophic cardiomyopathy
  • Indication to undergo cardiac magnetic resonance imaging (CMR) according to current ESC guidelines
  • Age 18 years or older
  • Written informed consent obtained
Not Eligible

You will not qualify if you...

  • History of previous myocardial infarction or myocardial revascularization (coronary artery bypass grafting or percutaneous coronary angioplasty)
  • Evidence of coronary artery stenosis 50% or greater on coronary CT scan or invasive coronary angiography

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Baseline and after 36 months

Participants undergo cardiac magnetic resonance imaging (CMR) to assess myocardial perfusion and characterize hypertrophic cardiomyopathy phenotypes.

2 visits (in-person)

Long-term Monitoring

Duration - 36 months

Participants are monitored over time to evaluate changes in myocardial perfusion and disease progression.

Follow-up visit after 36 months

Trial Site Locations

Total: 1 location

1

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Bologna, BO, Italy, 40124

Actively Recruiting

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Research Team

L

Luigi Lovato

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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