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NCT06888271Possibly a fitNot yet recruiting

DNA changes in Brugada syndrome and sudden cardiac death risk

Brugada SyndromeSudden Cardiac Death Due to Cardiac Arrhythmia

Part of Genetic & congenital, Heart & circulation clinical trials.

This study looks at DNA changes in people with Brugada syndrome to better understand who might be at risk for sudden cardiac death. By analyzing a blood sample, researchers hope to find markers that could improve risk prediction.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
10 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You must be 18 or older.
  • You must have a confirmed Brugada syndrome diagnosis, shown by a type 1 pattern on an ECG (either naturally or after a medication test).
  • You must not have any other structural heart disease.
  • You and other blood relatives in this trial cannot both participate.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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