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Biology of Juvenile Myoclonic Epilepsy
Sponsor: King's College London
Summary
The investigators are collecting genetic information through blood samples as well as clinical and EEG data from over 1000 people with Juvenile Myoclonic Epilepsy (JME) across the UK, Europe and North America. This study will draw on both existing and new samples from JME patients. These will be compared to anonymised data from samples for 2000 controls. The goal of this study is to find the genetic cause of JME. Finding the cause will help create better treatments for JME, as well as improve patient outcomes by allowing us to detect it earlier.
Key Details
Gender
All
Age Range
10 Years - 40 Years
Study Type
OBSERVATIONAL
Enrollment
1000
Start Date
2017-07-13
Completion Date
2026-12-31
Last Updated
2025-09-05
Healthy Volunteers
No
Conditions
Interventions
Blood draw
Participation includes one visit for one blood draw per recruited patient. 10-20ml peripheral venous blood will be taken from the antecubital fossa. The DNA from the blood sample will then be extracted and resequenced for analysis.
Existing samples
Control DNA samples will be used that have been previously acquired in other studies.
Locations (15)
Mount Sinai-Beth Israel Medical Center
New York, New York, United States
St Luke's Roosevelt Hospital
New York, New York, United States
Nationwide Children's Hospital
Columbus, Ohio, United States
Hospital for Sick Kids
Toronto, Ontario, Canada
Charles University
Prague, Czechia
Danish National Epilepsy Centre
Dianalund, Denmark
Tallinn Children's Hospital
Tallinn, Estonia
University Robert Debré
Paris, France
Commissione Genetica Lega Italiana contro l'Epilepssia
Roma, Italy
Vestre Viken Health Trust, Oslo
Drammen, Norway
Walton Centre for Neurology and Neurosurgery
Liverpool, United Kingdom
Royal London Hospital
London, United Kingdom
St Thomas' Hospital
London, United Kingdom
King's College Hospital NHS Trust
London, United Kingdom
Swansea University
Swansea, United Kingdom