National Network for Cardiovascular Genomics: Advancing Cardiovascular Healthcare for Hereditary Diseases in Brazil's Unified Health System Through a Multicenter Registry

Recruiting now

Conditions studied: Cardiomyopathy, Hypertrophic, Cardiomyopathy, Dilated, Cardiomyopathy Restrictive, Arrhythmogenic Right Ventricular Dysplasia, Non-Compaction Cardiomyopathy, Familial Hypercholesterolemia, Marfan Syndrome, Ehlers-Danlos Syndrome, Vascular Type, Loeys-Dietz Syndrome, Long QT Syndrome, Short Qt Syndrome, Brugada Syndrome, Catecholaminergic Polymorphic Ventricular Tachycardia, Sudden Cardiac Death

In brief

The goal of this observational study is to develop a registry of Brazilian patients with hereditary cardiovascular diseases, combining clinical and genomic data. The main questions it aims to answer are: Which genes are most commonly affected? What is the frequency of these genetic alterations in our population? Participants will be interviewed in routine medical care visits and their DNA will be sequenced.

Key facts

Study ID
NCT06546137
Run by
Hospital do Coracao
People needed
1211
Starts
2025-04-30
Expected to finish
2026-08-31
Last updated by the study team
2026-05-08

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.