Clin2
NCT06546137Possibly a fitRecruiting

Registry for inherited heart conditions in Brazil

Cardiomyopathy, HypertrophicCardiomyopathy, DilatedCardiomyopathy RestrictiveArrhythmogenic Right Ventricular DysplasiaNon-Compaction CardiomyopathyFamilial HypercholesterolemiaMarfan SyndromeEhlers-Danlos Syndrome, Vascular Type

Part of Blood & lymphatic, Bones, joints & muscles, Genetic & congenital, Heart & circulation, Hormones & metabolism, Skin clinical trials.

This study is building a national registry in Brazil to learn more about inherited heart conditions and improve care. If you have a family-related heart disease, you may be able to join and help advance cardiovascular healthcare.

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

Phase
N/A
Enrollment
1,211 people
Ages
Any age
Study type
Observational

Who can take part

  • You have a hereditary (inherited) heart condition, like certain types of cardiomyopathy or arrhythmia.
  • You agree to receive genetic counseling to learn about your condition and family risks.
  • You sign a consent form to join the study.
  • You provide the information the study asks for, like your medical history.

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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