I63.9 G40.9
Conditions
Interventions
Group 1: Patients receive an EEG measurement with dry electrode EEG caps within seven days of a cerebrovascular event. In study visits after 90 days and two years and in anual telephone interviews, pa
Sponsors
Charité Campus Benjamin Franklin
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: acute cerebrovascular disorders (trigger event), defined by: i) a transient ischemic attack (TIA) with clinical restitution within 24h AND initial neurological deficit verified by a neurologist OR ABCD2-Score >= 3 OR visibleDWI-lesion (MRI) OR the main hospital diagnosis of Amaurosis fugax ii) Ischemic stroke including retinal central artery occlusion iii) stroke caused by non-traumatic intracerebral hemorrhage iv) stroke caused by cerebral venous thrombosis
Exclusion criteria
Exclusion criteria: Epileptic seizure prior to the event leading to inclusion in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1st: Development of seizures, diagnosed using Epilepsy-Screening questionnaire by Ottman et al. 2nd: Development of Post-Stroke Depression using PHQ-9 questionnaire 3rd: Development of post-stroke cognitive decline using Montreal cognitive assessment (MOCA)-test | — |
Secondary
| Measure | Time frame |
|---|---|
| Development of acute symptomatic seizures within 7 days after the cerebrovascular event | — |
Countries
Germany
Contacts
Public ContactJakob Dörrfuß
Charité Universitätsmedizin BerlinKlinik für Neurologie
Outcome results
None listed