Clin2
NCT06794710Possibly a fitNot yet recruiting

Finding and treating rare heart muscle diseases early

Hypertrophic Cardiomyopathy (HCM)Dilated Cardiomyopathy (DCM)Metabolic CardiomyopathyRestrictive Cardiomyopathy

Part of Genetic & congenital, Heart & circulation clinical trials.

This study aims to find and treat rare types of heart muscle disease early. If you have heart failure but no known heart disease, researchers will use MRI and other tests to see if a rare cause is behind your symptoms and then offer targeted treatment.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
300 people
Ages
18 years to 75 years
Study type
Interventional

Who can take part

  • You must be between 18 and 75 years old.
  • You have been diagnosed with heart failure and are about to start drug therapy.
  • You have not had heart disease in the past (like blocked arteries, valve problems, or birth defects).
  • Your kidneys must be working well enough (a kidney clearance test result of 50 or higher).
  • Your heart's pumping ability should be preserved (ejection fraction of at least 50%).
  • You must be able to have an MRI safely.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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