Clin2
NCT06794710Possibly a fitNot yet recruiting

Early detection and treatment of rare heart muscle diseases

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

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

This study looks at people who have been newly diagnosed with heart failure to find rare forms of heart muscle disease (cardiomyopathy) early and start the right treatment. It uses advanced heart imaging (CMR) and requires that you have not had heart problems before.

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 are between 18 and 75 years old.
  • You have heart failure that has just been found, and your doctor is planning to start you on heart medications.
  • You have no known history of heart disease, including blocked arteries, valve problems, or heart muscle damage.
  • Your kidney function is good (creatinine clearance at least 50 ml/min).
  • Your heart's pumping ability is normal or nearly normal (LVEF 50% or higher).
  • You agree to have a special MRI of your heart (CMR) and sign a consent form.

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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