Clin2
NCT02432092Possibly a fitRecruiting

Genetic testing for heart muscle disease in children and families

CardiomyopathiesDilated CardiomyopathyHypertrophic CardiomyopathyRestrictive CardiomyopathyArrhythmogenic Right Ventricular CardiomyopathyLeft Ventricular Non-compaction Cardiomyopathy

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

This study looks at genetic (DNA) changes that may cause cardiomyopathy, a disease where the heart muscle is weakened. It may help families understand possible causes and inform future care.

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

Phase
N/A
Enrollment
300 people
Ages
Any age
Study type
Observational

Who can take part

  • You or your child must have cardiomyopathy (heart muscle disease)
  • If you’re not the patient, you must be a close family member of someone with cardiomyopathy
  • People without cardiomyopathy are not eligible
  • Family members of someone without cardiomyopathy are not eligible

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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