Condition: Juvenile Myoclonic Epilepsy · Sponsor: King's College London
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.
This description comes directly from the study's public registry record.
Deb K Pal, MD PhD · +442078480608 · deb.pal@kcl.ac.uk
Always discuss trial participation with your own doctor first.
| Mount Sinai-Beth Israel Medical Center | New York, New York, United States | Completed |
| St Luke's Roosevelt Hospital | New York, New York, United States | Completed |
| Nationwide Children's Hospital | Columbus, Ohio, United States | Completed |
| Hospital for Sick Kids | Toronto, Ontario, Canada | Recruiting |
| Charles University | Prague, Czechia | Recruiting |
| Danish National Epilepsy Centre | Dianalund, Denmark | Recruiting |
| Tallinn Children's Hospital | Tallinn, Estonia | Recruiting |
| University Robert Debré | Paris, France | Recruiting |
| Commissione Genetica Lega Italiana contro l'Epilepssia | Roma, Italy | Recruiting |
| Vestre Viken Health Trust, Oslo | Drammen, Norway | Recruiting |
| Walton Centre for Neurology and Neurosurgery | Liverpool, United Kingdom | Recruiting |
| Royal London Hospital | London, United Kingdom | Recruiting |
+ 3 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT03400371