Epilepsy
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • Diagnosis of Rolandisch epilepsy, ESES, ESES-like or Landau-Kleffner syndrome • Age of 8 to 18 years • Clinical and electroencephalographic evidence of seizures. • Non-symptomatic epilepsy;Healthy control group Inclusion criteria for healthy control children: • Children aged 8 to 16 years • Normal intelligence/following regular schools
Exclusion criteria
Exclusion criteria: • MRI lesions on previous structural brain MRI- or CT-scans or symptomatic epilepsy (e.g. tumours, vascular abnormalities, congenital dysgenesia) • Progressive neurological disorders • Other diseases/ causes that may underlie cognitive impairment (i.e. psychiatric diseases) • Vision less than +4.5D or - 4.5D • Claustrophobia • Metal implants or other contraindication for MRI • Parents not willing to provide informed consent;Healthy control children Exclusion criteria for the healthy control children: • Medical history of head trauma or other diseases/ causes that may underlie cognitive impairment (i.e. psychiatric diseases) • Inability to speak/understand the Dutch language • Vision less than +4.5D or - 4.5D • Claustrophobia • Metal implants or other contraindication for MRI • Parents not willing to provide informed consent • Parents who do not want to get informed whenever structural abnormalities are found during imaging
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Abnormalities that are related to Rolandic epilepsy, ESES-like, ESES, LKS, language impairment, cognitive impairment and/or refractoriness. Endpoints are the microstructural and functional integrity, seizure history, IQ-scores, and response to anti-epileptic drug treatment or other treatment (corticosteroids), EEG-parameters (localisation and frequency of epileptic activity). (For further information see: Methods, primary study parameters/endpoints) | — |
Secondary
| Measure | Time frame |
|---|---|
| nvt | — |
Countries
Netherlands