PATient based phenotyping and evaluation of therapy for Rare Epilepsies
- Conditions
- genetic epilepsyORPHA:101998 Rare epilepsyORPHA:544254 SYNGAP1-related developmental and epileptic encephalopathyG40Epilepsy
- Registration Number
- DRKS00032075
- Lead Sponsor
- Institut für Rehabilitation, Transition und Palliation von neurologisch kranken Kindern der Paracelsus Medizinischen Privatuniversität Salzburg an der Schön Klinik Vogtareuth
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Enrolling by invitation
- Sex
- All
- Target Recruitment
- 3000
Inclusion Criteria
confirmed diagnosis of genetic epilepsy or related ion channel disease
Exclusion Criteria
not applicable
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Registry / Natural history study<br>The PATRE study aims to establish a patientbased database and registry focused on genetic epilepsies.
- Secondary Outcome Measures
Name Time Method observational cohort study / registry<br>(no secundary outcome)