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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Gene Expression Changes of Brain Tissue in Human Temporal Lobe Epilepsy With Hippocampal SclerosisCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hippocampal Sclerosis, Malformations of Cortical Development, Group I, brain disorder, central nervous system disorder, central nervous system malformation, cerebral cortical dysplasia, epilepsy, nervous system disorderActive, not recruitingNot stated2026-04-27NCT04917939