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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Epilepsy Epilepsies, Myoclonic Myoclonic Epilepsy, Juvenile
This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.
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.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
You can take part if:
You may not be able to take part if:
This is in the inclusion criteria above
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Deb K Pal, MD PhD
+442078480608
deb.pal@kcl.ac.uk
The study is sponsored by King's College London and is in collaboration with King's College Hospital NHS Trust; Charles University, Czech Republic; Hopital Universitaire Robert-Debre; Vestre Viken Hospital Trust; The Hospital for Sick Children; Cardiff University; Odense University Hospital.
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
You can print or share the study information with your GP/healthcare provider or contact the research team directly.