Comparison of the quality of mobile and clinical EEGs

• Conditions: EEG study; G40; Epilepsy

• Registration Number: DRKS00012424
• Lead Sponsor: Institut für Medizinische Informatik, RWTH Aachen, Uniklinik Aachen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-07-11
• Study Completion: 2018-05-18
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 22

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

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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.