Condition: SCN1A · Dravet Syndrome · Epilepsy · Sponsor: NHS Greater Glasgow and Clyde
The aims of this prospective natural history study are to define the seizure, neuro-developmental, and behavioural characteristics of SCN1A-related epilepsies/Dravet syndrome in children and adults longitudinally over a period of three years. In addition, this study will compare missense and truncating genotypes in terms of i) rates of change of countable convulsive seizures per month and ii) neurodevelopmental outcome and trajectories.
This description comes directly from the study's public registry record.
Kirsty Hendry, PhD · 0141 451 5888 · SCN1AHorizons@glasgow.ac.uk
Andreas Brunklaus, MD PhD · 0141 451 5888 · andreas.brunklaus@glasgow.ac.uk
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| Royal Hospital for Children | Glasgow, United Kingdom | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06504511