ClinicalTrials.gg
RecruitingNCT06546137RENOMICA-HcorUpdated May 8, 2026

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

An observational study in Cardiomyopathy, Hypertrophic, Cardiomyopathy, Dilated and Cardiomyopathy Restrictive, sponsored by Hospital do Coracao. Recruiting at 27 sites in Brazil. Per ClinicalTrials.gov, last updated 2026-05-08.

Sponsored by Hospital do Coracao · Observational

From the registry’s dates

  • Started Apr 2025; still recruiting 1 year 6 months later.
Study type
Observational
Model
Family-based
Time perspective
Prospective
Enrollment
1,211
Sex
All
01

Study 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.

02

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

Keywords

  • hereditary cardiovascular diseases
  • whole genome sequencing
03

In context

Cardiomyopathy, Hypertrophic

363 studies on the registry are indexed under Cardiomyopathy, Hypertrophic; 116 are open to participants now.

This study's planned enrollment of 1,211 is above the median of 259 across 174 observational studies indexed under Cardiomyopathy, Hypertrophic.

Browse Cardiomyopathy, Hypertrophic studies →

Lead sponsor

Hospital do Coracao is the lead sponsor of 67 studies on the registry; 14 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients under routine medical care in hospitals and clinics located in Brazil with a clinical diagnosis of an hereditary cardiovascular disease.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Clinical diagnosis of a hereditary cardiovascular disease according to current clinical guidelines
  • Agree to receive genetic counseling
  • Sign form
  • Provide the information required in the case report form

Exclusion criteria

Exclusion Criteria:

  • Signature absent from form
  • Inadequate buccal swab (sample may be collected twice)
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Family-based
Time perspective
Prospective
Enrollment
1,211 participants (estimated)
Target follow-up
6 Months
Patient registry
Yes
Biospecimen retention
Samples with dna

Interventions

  • Diagnostic testwhole genome sequencing

    whole genome sequencing of genomic DNA extracted from buccal swab

06

What researchers measure

Primary outcomes

  1. Diagnostic yield

    Percentage of participants with pathogenic or likely pathogenic variants

    Time frame: 30 months after study start date

  2. Genetic diversity

    Determine genes that cause hereditary cardiovascular diseases in Brazil

    Time frame: 30 months after study start date

  3. Variant frequency

    Determine the frequency of disease-causing and benign variants in the Brazilian population

    Time frame: 30 months after study start date

07

Study locations

27 of 27 sites recruiting
  • Centro de Pesquisa Silvestre Santé
    Rio Branco, Acre 69915-030, Brazil
    Recruiting
    • Odilson Marcos Silvestre · Contactodilsonms@gmail.com · +5568999211100
    • Odilson Marcos Silvestre · Principal investigator
  • Centro de Pesquisas Clínicas Dr. Marco Mota
    Maceió, Alagoas 57051-160, Brazil
    Recruiting
    • Marco Antonio Mota Gomes · Contactmota-gomes@uol.com.br · +558232155066
    • Marco Antonio Mota Gomes · Principal investigator
  • Hospital Universitário da Unifap
    Macapá, Amapá 68903-419, Brazil
    Recruiting
  • Hospital de Messejana Dr. Carlos Alberto Studart Gomes
    Fortaleza, Ceará 60840-285, Brazil
    Recruiting
    • Sônia Maria Cavalcante da Rocha · Contactsonia.mrcavalcante@gmail.com · +558531014151
    • Sônia Maria Cavalcante da Rocha · Principal investigator
  • Hospital Evangélico de Vila Velha
    Vila Velha, Espírito Santo 29118-060, Brazil
    Recruiting
    • Carina Laranja Mattos Barreto · Contactclaranjamattos@gmail.com · +552799513-6656
    • Carina Laranja Mattos Barreto · Principal investigator
  • Hospital Universitário Professor Edgard Santos
    Salvador, Estado de Bahia 40110-060, Brazil
    Recruiting
    • Luiz Pereira de Magalhães, MD PhD · Contactluizmagalhaes12@gmail.com · +557136463400
    • Luiz Pereira de Magalhães · Principal investigator
  • Hospital Ana Nery - HAN/SESAB
    Salvador, Estado de Bahia 40320-010, Brazil
    Recruiting
  • Instituto de Cardiologia e Transplantes do Distrito Federal
    Brasília, Federal District 70675-731, Brazil
    Recruiting
    • Cristina Machado Camargo Afiune · Contactcris.afiune@gmail.com · +556134511000
    • Cristina Machado Camargo Afiune · Principal investigator
  • Hospital das Clínicas da Universidade Federal de Goiás - HC-UFG
    Goiânia, Goiás 74605-050, Brazil
    Recruiting
    • Weimar Kunz Sebba Barroso de Souza · Contactsebbabarroso@gmail.com · +556232698200
    • Weimar Kunz Sebba Barroso de Souza · Principal investigator
  • Hospital Felicio Rocho - HFR
    Belo Horizonte, Minas Gerais 30110-934, Brazil
    Recruiting
    • Maria da Consolação Vieira Moreira · Contactmariacvmoreira@gmail.com · +553135147000
    • Maria da Consolação Vieira Moreira · Principal investigator
  • Liga Mineira de Ressuscitação Cardiopulmonar
    Belo Horizonte, Minas Gerais 30130-110, Brazil
    Recruiting
  • Santa Casa de Misericórdia de Montes Claros
    Montes Claros, Minas Gerais 39401-001, Brazil
    Recruiting
  • Health & Care
    Belém, Pará 66093-055, Brazil
    Recruiting
  • Hospital Universitário Pedro Ernesto - UERJ
    Rio de Janeiro, Rio de Janeiro 20551-030, Brazil
    Recruiting
  • Instituto de Puericultura e Pediatria Martagão Gesteira
    Rio de Janeiro, Rio de Janeiro 21941-912, Brazil
    Recruiting
    • Nathalie J. M. Bravo Valenzuela · Contactnjmbravo@cardiol.br · +552139384816
    • Nathalie J. M. Bravo Valenzuela · Principal investigator
  • Hospital Universitário Clementino Fraga Filho - UFRJ
    Rio de Janeiro, Rio de Janeiro 21941-913, Brazil
    Recruiting
    • Tais Hanae Kasai Brunswick · Contactkasaitais@biof.ufrj.br · +552139382789
    • Tais Hanae Kasai Brunswick · Principal investigator
  • Instituto Nacional de Cardiologia
    Rio de Janeiro, Rio de Janeiro 22240-006, Brazil
    Recruiting
    • Helena Cramer Veiga Rey, MD PhD · Contacthcramer0504@gmail.com · +552130372105
    • Helena Cramer Veiga Rey · Principal investigator
  • Hospital Universitário Onofre Lopes - UFRN
    Natal, Rio Grande do Norte 59012-300, Brazil
    Recruiting
    • Rosiane Viana Zuza Diniz · Contactrosianevzdiniz@gmail.com · +558433425000
    • Rosiane Viana Zuza Diniz · Principal investigator
  • Hospital das Clínicas de Porto Alegre - UFRGS
    Porto Alegre, Rio Grande do Sul 90035-903, Brazil
    Recruiting
    • Fabiano de Oliveira Poswar · Contactfposwar@hcpa.edu.br · +555133598000
    • Fabiano de Oliveira Poswar · Principal investigator
  • Instituto de Cardiologia - Fundação Universitária de Cardiologia de Porto Alegre - IC-FUC
    Porto Alegre, Rio Grande do Sul 90040-370, Brazil
    Recruiting
  • Instituto de Pesquisa e Ensino em Saúde - IPES
    Porto Velho, Rondônia 76801-098, Brazil
    Recruiting
    • Mariana Pinheiro Alves Vasconcelos · Contactdbpfall@gmail.com · +5569993787257
    • Mariana Pinheiro Alves Vasconcelos · Principal investigator
  • Centro Multidisciplinar de Ensino Especializado e Pesquisa Ltda
    Joinville, Santa Catarina 89204-250, Brazil
    Recruiting
    • Kárila Scarduelli Luciano · Contactkarilasl@gmail.com · +5547992007079
    • Kárila Scarduelli Luciano · Principal investigator
  • Hospital Universitário São Francisco na Providência de Deus, USF-SP
    Bragança Paulista, São Paulo 12916-542, Brazil
    Recruiting
  • Instituto PENSI
    Consolação, São Paulo 01228-200, Brazil
    Recruiting
  • Hospital Universitário da Universidade Federal de São Carlos
    São Carlos, São Paulo 13566-448, Brazil
    Recruiting
  • Hospital do Coracao
    São Paulo, São Paulo 04004-030, Brazil
    Recruiting
  • Universidade Federal do Tocantins
    Palmas, Tocantins 77001-090, Brazil
    Recruiting
08

References and documents

Individual participant data

Plan to share: No — Genomic data are sensitve and will not be shared for individual participants

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Apr 2025 (actual). Primary completion is estimated for Aug 2026, 16 months after the start.

Of 82 observational studies under Cardiomyopathy, Hypertrophic, half reached primary completion within 85 months of starting (the median), counting those still running; a quarter within 43. This study's planned 16 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 6, 2024
First posted
Aug 9, 2024
StartActual
Apr 30, 2025
Primary completionEst.
Aug 31, 2026
CompletionEst.
Aug 31, 2026
Last update
May 8, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06546137
Lead sponsor
Hospital do Coracao
Collaborators
Instituto Nacional de Cardiologia de Laranjeiras, Universidade Federal do Rio de Janeiro
Responsible party
Sponsor
First posted
Aug 9, 2024
Start date
Apr 30, 2025
Primary completion
Aug 31, 2026 (estimated)
Completion
Aug 31, 2026 (estimated)
Last update
May 8, 2026

Study contacts

Adriana Bastos Carvalho, MD PhD
Contact
carvalhoab@biof.ufrj.br
+552130372105

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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