RareWays is a research directory. It helps you understand the science. It is not medical advice. Always discuss your care options with your healthcare team.
Coverage: 2020-01-01 onwards, with up to 300 results per query from PubMed and Europe PMC and separate limits on other sources. This is a selected index, not a complete literature search.
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Brugada Syndrome: Research Summary
Printed from RareWays (rareways.org)
For general awareness only. Not medical advice. Discuss all care options with your healthcare team.
5 Most Recent Research Articles
- 1.
Genetic characterisation of Brugada Syndrome in Malaysia: Clinical and SCN5A variant insights
N.A. Seman et al., International Journal of Cardiology (17 October 2026)
https://doi.org/10.1016/j.ijcard.2026.134915
- 2.
The Brugada Syndrome: Is Provocative Testing Necessary?
Naccarelli Gerald V, The American journal of cardiology (15 October 2026)
https://pubmed.ncbi.nlm.nih.gov/42600724/
- 3.
Unmasking brugada syndrome: Baseline r′-wave triangle base duration and beta-angle in oral flecainide challenge positivity
Sunu Budhi Raharjo et al., Heart Science Journal (13 October 2026)
https://doi.org/10.21776/ub.hsj.2026.007.04.10
- 4.
The ARumenamide AR-788 suppresses the transient outward current in human iPSC-derived right-ventricular Brugada cardioids
Yohan Gueret et al., medRxiv (8 October 2026)
https://doi.org/10.64898/2026.10.06.26364857
- 5.
Oscillatory Epicardial Delayed Potentials and Associated Unipolar Voltage Gradients in Brugada Syndrome.
Nagase Satoshi et al., JACC. Clinical electrophysiology (8 October 2026)
https://pubmed.ncbi.nlm.nih.gov/42886096/
Source: RareWays research directory. Data from PubMed, Europe PMC, OpenAlex, ClinicalTrials.gov.
Always verify information with your healthcare team before making any decisions about your care.
Brugada Syndrome
Brugada syndrome is a rare inherited heart rhythm disorder that can cause dangerous fast heartbeats from the lower chambers of the heart. It may lead to fainting, cardiac arrest or sudden death, often at rest or during sleep or fever. It is diagnosed using a characteristic ECG pattern. Management includes avoiding triggers such as fever and certain medicines, and an implantable defibrillator for people at high risk.
This overview is general information, not an individual medical assessment. Research is selected automatically and may include mismatches. How we select and explain research.
Most Recent Research
Common Questions
What is Brugada Syndrome?
Brugada syndrome is a rare inherited heart rhythm disorder that can cause dangerous fast heartbeats from the lower chambers of the heart. It may lead to fainting, cardiac arrest or sudden death, often at rest or during sleep or fever. It is diagnosed using a characteristic ECG pattern. Management includes avoiding triggers such as fever and certain medicines, and an implantable defibrillator for people at high risk.
How many clinical trials are available for Brugada Syndrome?
RareWays currently indexes 18 clinical trials for Brugada Syndrome, of which 1 is actively recruiting. These counts cover indexed trials across countries, not just your country. An Australian site does not necessarily mean that site is recruiting. Check locations, eligibility and current availability with the study team.
Where does the research data for Brugada Syndrome come from?
RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is refreshed automatically every day. All articles and trials link directly to their original sources.
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