Clin2
NCT02824822Possibly a fitRecruiting

Genetic test study for heart rhythm risk in people with seizures

EpilepsySeizuresSyncopeChannelopathyCardiomyopathies

Part of Brain & nervous system, Genetic & congenital, Heart & circulation clinical trials.

This study checks whether genetic markers are linked to heart rhythm problems in people with epilepsy or seizure-related events, and in some close relatives. It may help doctors better spot who is at risk for dangerous heart rhythm issues.

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

Phase
N/A
Enrollment
600 people
Ages
18 years to 50 years
Study type
Observational

Who can take part

  • Be an adult age 18 to 50
  • Have epilepsy or seizures, or have had fainting (syncope), drowning, cardiac arrest, sudden death, or an abnormal ECG suggesting an arrhythmia
  • OR be a blood relative (parent, sibling, child, etc.) of someone with epilepsy, seizures, cardiac arrest, sudden death, drowning, fainting, or a heart rhythm problem
  • Be able and willing to sign written consent
  • Not have seizures caused by lack of blood flow to the brain (ischemic events)
  • Not have a history of traumatic brain injury with seizures or prior brain surgery or a brain tumor

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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