Diagnostic and therapeutic yield of a patient controlled portable EEG device with dry electrodes (Fourier One) in home-monitoring of neurological outpatients

Diagnostic and therapeutic yield of a patient controlled portable EEG device with dry electrodes (Fourier One) in home-monitoring of neurological outpatients - Home

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00012685

Enrollment

600

Registered

2017-08-09

Start date

2017-05-22

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

portable EEG recorder in home monitoring disturbances of consciousness

Interventions

Group 1: In the first phase of the study (feasibility study), both the portable EEG device and the conventional EEG are used in the practices of neurologists. Group 2: In the second phase (home moni

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients in the doctors office with a medical indication to record a conventional EEG

Exclusion criteria

Exclusion criteria: patients <18 years

Design outcomes

Primary

Measure	Time frame
Technical signal quality as described by amplitude and noise measures (visual evaluation only)	—

Secondary

Measure	Time frame
Change of management induced by the evaluation of the ambulatory EEG recording All documentation of the practicing physicians before and after EEG will be read twice by neurologists of the university clinic (possibly diagnosis enhancement).	—

Countries

Germany

Contacts

Public ContactHans-Jochen Heinze

Otto-von-Guericke-Universität Magdeburg Medizinische Fakultät Klinik für Neurologie

kneu@med.ovgu.deTel.+49 391 6713431

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 6, 2026