Clin2
NCT05100420Possibly a fitEnrolling by invitation

HCM registry and DNA/imaging data collection study

Hypertrophic CardiomyopathyHypertrophic Obstructive CardiomyopathyFamilial Hypertrophic CardiomyopathyCardiomyopathies

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

This study collects health records, heart ultrasound (echo), MRI images, and optional DNA testing for people with hypertrophic cardiomyopathy (HCM). It aims to build a large database to better understand HCM and support future research and care.

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

Phase
N/A
Enrollment
2,000 people
Ages
Any age
Study type
Observational

Who can take part

  • You have a clinical diagnosis of hypertrophic cardiomyopathy (HCM), or a known HCM-causing gene change
  • If you’re diagnosed through family history or heart scans, your clinician must meet specific heart-thickness criteria
  • If you’re a gene carrier, the genetic test must be for certain sarcomere genes and labeled “pathogenic” or “likely pathogenic” by a certified lab
  • You should not have Noonan syndrome or related “Rasopathy” conditions
  • You should not have other inherited heart muscle diseases (for example Fabry, Pompe, Danon, or carnitine-related disorders)
  • You must be able to consent and upload an echocardiogram and/or cardiac MRI images for review

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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