Quantitative EEG as biomarker for the prediction of seizures, depression and cognitive decline after stroke - A substudy to the Berling Longterm Observation of Vascular Events - BeLOVE - Study
- Conditions
- I63.9G40.9Cerebral infarction, unspecifiedEpilepsy, unspecified
- Registration Number
- DRKS00017079
- Lead Sponsor
- Charité Campus Benjamin Franklin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 625
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
Epileptic seizure prior to the event leading to inclusion in the study
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1st: Development of seizures, diagnosed using Epilepsy-Screening questionnaire by Ottman et al.<br>2nd: Development of Post-Stroke Depression using PHQ-9 questionnaire<br>3rd: Development of post-stroke cognitive decline using Montreal cognitive assessment (MOCA)-test<br>
- Secondary Outcome Measures
Name Time Method Development of acute symptomatic seizures within 7 days after the cerebrovascular event