Clinical Trial

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

Study acronym: RENOMICA-Hcor
Recruiting
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Summary
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.
Protocol Amendment History 1 change
notable Enrollment increased: 600 -> 1211 participants 2026-05-09
Trial Details
NCT Number NCT06546137
Lead Sponsor Hospital do Coracao
Collaborators: Instituto Nacional de Cardiologia de Laranjeiras, Universidade Federal do Rio de Janeiro
Conditions Cardiomyopathy, Hypertrophic, Cardiomyopathy, Dilated, Cardiomyopathy Restrictive, Arrhythmogenic Right Ventricular Dysplasia, Non-Compaction Cardiomyopathy, Familial Hypercholesterolemia, Marfan Syndrome, Ehlers-Danlos Syndrome, Vascular Type +6 more
Enrollment 1,211 participants
Start Date 2025-04-30
Primary Completion 2026-08-31 (estimated)
Study Completion 2026-08-31 (estimated)
Updated on ClinicalTrials.gov 2026-05-08