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The Rolandic epilepsy/ESES/Landau-Kleffner Syndrome and correlation with Language impairment study

The Rolandic epilepsy/ESES/Landau-Kleffner Syndrome and correlation with Language impairment study - REL&language1

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON36427
Enrollment
45
Registered
2010-08-09
Start date
2010-10-29
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epilepsy

Interventions

None listed

Sponsors

Epilepsiecentrum Kempenhaeghe
Lead Sponsor

Eligibility

Age
2 Years to 17 Years

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

MeasureTime 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

MeasureTime frame
nvt

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)