EEG study G40
Conditions
Interventions
Group 1: Mobile EEG examination for about 30 minutes with resting EEG, EEG in hyperventilation and EEG with closed eyes.
Parallel data acquisition with mobile EEG and permanent, stationary video EEG
Sponsors
Institut für Medizinische Informatik, RWTH Aachen, Uniklinik Aachen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Patients who currently receive a classical EEG examination on the ward 2. No time difference between standard EEG and mobile EEG 3. Majority Age 4. Written declaration of consent 5. legal competence 6. Persons who are able to work and are mentally able to follow the instructions of the study staff
Exclusion criteria
Exclusion criteria: 1. Patients who have cardiological or neurological implants (heart pacemaker, defibrillator, cochlear implants, etc.) 2. Patients with an acute wound or injury to the head or cervical spine 3. Persons placed under an official or judicial order in an institution 4. Persons who are in a dependency or employment relationship with the sponsor or auditor 5. Simultaneous participation in another clinical trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Detection of epilepsy-typical pathological potentials with mobile EEG devices in patients with a known epilepsy. The potentials should be able to withstand a significant comparison of mobile EEG devices in comparison to the classical EEG device. | — |
Countries
Germany
Contacts
Public ContactYannic Titgemeyer
Institut für Medizinische Informatik, RWTH Aachen, Uniklinik Aachen
Outcome results
None listed