Identifying genetic markers for Brugada Syndrome diagnosis

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This research focuses on improving the diagnosis of Brugada Syndrome (BrS) through advanced genetic sequencing techniques. By developing a genetic signature and identifying specific biomolecular profiles, the study aims to enhance understanding of the syndrome's molecular mechanisms. The approach includes a multi-omic strategy that integrates whole-exome sequencing and machine learning to uncover altered pathways related to BrS. The ultimate goal is to facilitate personalized treatment plans and refined risk assessment for patients affected by BrS.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age \> 18 years
* Patients affected by Brugada Syndrome
* Patients who signs the Informed Consent

Exclusion Criteria:

* None

Where it's running

• Irccs Policlinico San Donato
  San Donato Milanese, Milan, Italy Recruiting

Study contacts

• Study coordinator: Giuseppe Ciconte MD, PhD
• Email: Giuseppe.Ciconte@grupposandonato.it
• Phone: +390252774260

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.