Scientists hunt genetic clues in 1000 epilepsy patients
NCT ID NCT03400371
Summary
This study aims to discover the genetic causes of Juvenile Myoclonic Epilepsy (JME), a common form of epilepsy that starts in childhood. Researchers are collecting blood samples, medical information, and brainwave test results from 1000 people with JME across multiple countries. By comparing this data with people who don't have epilepsy, they hope to identify genetic patterns that could lead to better treatments and earlier detection in the future.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Charles University
RECRUITINGPrague, 116 36, Czechia
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Commissione Genetica Lega Italiana contro l'Epilepssia
RECRUITINGRoma, 00198, Italy
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Danish National Epilepsy Centre
RECRUITINGDianalund, 4293, Denmark
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Hospital for Sick Kids
RECRUITINGToronto, Ontario, M5G 0A4, Canada
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King's College Hospital NHS Trust
RECRUITINGLondon, SE5 9RS, United Kingdom
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Contact Email: •••••@•••••
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Mount Sinai-Beth Israel Medical Center
COMPLETEDNew York, New York, 10003, United States
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Nationwide Children's Hospital
COMPLETEDColumbus, Ohio, 43125, United States
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Royal London Hospital
RECRUITINGLondon, E1 1BZ, United Kingdom
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St Luke's Roosevelt Hospital
COMPLETEDNew York, New York, 10025, United States
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St Thomas' Hospital
RECRUITINGLondon, SE1 9HT, United Kingdom
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Swansea University
RECRUITINGSwansea, SA2 8PP, United Kingdom
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Tallinn Children's Hospital
RECRUITINGTallinn, 13419, Estonia
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University Robert Debré
RECRUITINGParis, 75019, France
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Vestre Viken Health Trust, Oslo
RECRUITINGDrammen, 3004, Norway
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Walton Centre for Neurology and Neurosurgery
RECRUITINGLiverpool, L9 7LJ, United Kingdom
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Conditions
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