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.

Similar studies

Other trials that look related to this one.

NCT03049254Recruiting
Registry and blood/tissue study for certain sudden heart death causes

This study builds a registry and collection of samples to better understand families affected by sudden heart death and related heart rhythm problems that are not clearly caused by a heart attack. It may help researchers identify patterns and improve future care, and it offers a way for patients and families to contribute to research.

Rochester, Minnesota
NCT07534163Not yet recruiting
Brazilian heart failure patient registry and tracking study

This study collects information from patients admitted to hospitals in Brazil with heart failure or a recent heart attack that weakened the heart. Researchers use this data to better understand heart failure patterns and improve treatment across the country.

NCT03880708Recruiting
Registry for inherited dangerous heart rhythm conditions

This study is a heart rhythm registry for people with inherited conditions that can cause abnormal heart beats. By collecting health and testing information, researchers hope to better understand these conditions and improve care.

Beijing, Beijing Municipality
NCT04189822Enrolling by invitation
Heart rhythm genetic registry and blood sample bio bank

This study is building a Canadian database and tissue/blood bank for people and families with inherited heart rhythm conditions (and some inherited heart muscle diseases). It collects consented health and genetic information to help researchers better understand who is at risk and how these conditions work.

Vancouver, British Columbia
NCT05871632Not yet recruiting
Cardiomyopathy registry for tracking heart disease

This study builds a patient registry to collect information over time about several types of cardiomyopathy (heart muscle diseases). It may help researchers understand how these conditions progress and what care works best.

Beijing, Beijing Municipality
NCT07257289Recruiting
Heart risk study for inherited heart conditions

This study looks at people with inherited heart diseases and their relatives to better predict risks of dangerous heart rhythms or heart failure. It may help find out if you or your family members need closer monitoring.

Bordeaux

Hear when a new Arrhythmogenic Right Ventricular Dysplasia trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.