Genetic and Electrophysiologic Study in Focal Drug-resistant Epilepsies | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Genetic and Electrophysiologic Study in Focal Drug-resistant Epilepsies	Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Craniofacial Abnormalities, Focal Cortical Dysplasia, Malformations of Cortical Development, Group I, Musculoskeletal Abnormalities, Neoplasms, Multiple Primary, Neuroinflammatory Diseases, brain disorder, central nervous system disorder, central nervous system malformation, cerebral cortical dysplasia, congenital hypothalamic hamartoma syndrome, encephalitis, epilepsy, focal epilepsy, hamartoma, hemimegalencephaly, hereditary disease, hereditary neoplastic syndrome, inherited neurodegenerative disorder, megalencephaly, musculoskeletal system disorder, neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, tuberous sclerosis	Recruiting	Not stated	2026-04-17		NCT02890641

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Organizations	Linked trials
Fondation Ophtalmologique Adolphe de Rothschild	81

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Research sites	City	Country	Linked trials
Fondation Ophtalmologique Adolphe de Rothschld	Paris	France	1