Brugada syndrome
MONDO:0015263A genetically heterogeneous condition characterized by complete or incomplete right bundle branch block accompanied by ST elevation in leads V1-V3. There is a high incidence of ventricular arrhythmia that may result in sudden death.
Also known as: Brugada syndrome, Brugada type idiopathic ventricular fibrillation, idiopathic ventricular fibrillation, Brugada type, right bundle branch block, ST segment elevation, and sudden death syndrome, sudden unexplained nocturnal death syndrome, sudden unexpected nocturnal death syndrome
41 clinical trials for this condition and its sub-types, 10 tagged with Brugada syndrome itself.
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Sub-types of Brugada syndrome
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Brugada syndrome 1 0 trials
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Brugada syndrome 3 0 trials
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Brugada syndrome 4 0 trials
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Brugada syndrome 5 0 trials
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Brugada syndrome 6 0 trials
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Brugada syndrome 7 0 trials
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Brugada syndrome 8 0 trials
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Brugada syndrome 9 0 trials
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Simple cheek swab could predict sudden cardiac death risk
Diagnosis Recruiting nowThis study explores whether a quick, painless cheek swab can spot protein changes linked to inherited heart conditions that cause sudden cardiac death in young people. Researchers will collect samples from 26 patients with arrhythmic disorders or family members at risk. If the te…
Sponsor: St. George's Hospital, London • Aim: Diagnosis
Last updated Jun 27, 2026 12:31 UTC
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Heart risk under the knife: new study tracks anesthesia dangers in rare cardiac condition
Knowledge-focused Recruiting nowThis observational study will follow 200 adults with Brugada Syndrome who need anesthesia for surgery or other procedures. Researchers want to see how often dangerous heart rhythms occur during and up to 30 days after anesthesia. They will also check if certain anesthetic drugs o…
Sponsor: Hospital Clinic of Barcelona • Aim: Knowledge-focused
Last updated Sep 10, 2026 00:00 UTC
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New registry aims to solve mystery of sudden child deaths
Knowledge-focused Recruiting nowThis study collects medical records, circumstances, and DNA from children who died suddenly and unexpectedly between ages 11 months and 18 years. Researchers will analyze this information to find risk factors and causes, with the goal of preventing future deaths. Families of affe…
Sponsor: NYU Langone Health • Aim: Knowledge-focused
Last updated Aug 30, 2026 00:00 UTC
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Brazil launches massive heart gene hunt to unlock hereditary mysteries
Knowledge-focused Recruiting nowThis study is building a registry of 1,211 people in Brazil who have inherited heart conditions like cardiomyopathy, arrhythmias, and Marfan syndrome. Researchers will collect DNA samples and medical information to discover which genes are most commonly affected and how often the…
Sponsor: Hospital do Coracao • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:30 UTC
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New fetal heart monitor could unlock secrets of stillbirth
Knowledge-focused Recruiting nowThis study is testing a new, non-invasive monitor (fetal magnetocardiography) to detect hidden heart problems in high-risk pregnancies that might lead to fetal death. Researchers will study 30 pregnant women with conditions like congenital heart disease or twin pregnancy. The goa…
Sponsor: Medical College of Wisconsin • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:10 UTC