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Identification of biomarkers for ambulatory and automated seizure detection.

Identification of biomarkers for ambulatory and automated seizure detection. - Automated seizure detection

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00026984
Enrollment
60
Registered
2021-10-26
Start date
2021-02-04
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

G40

Interventions

Group 1: Continuous collection of clinical data in order to identify recurrent patterns or digital biomarkers based on ECG and motion data for automated detection of epileptic seizures in the outpatie

Sponsors

Klinik für Neurologie/Sektion Epileptologie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 105 Years

Inclusion criteria

Inclusion criteria: Epileptic seizures, minimum 24-hour stay in Epilepsy Monitoring Unit.

Exclusion criteria

Exclusion criteria: Children (under 15 years of age), patients with open wounds in the area of attachment (under the chest), patients wearing a pacemaker, implantable cardioverter defibrillator (ICD) or other electronic implant.

Design outcomes

Primary

MeasureTime frame
Determine sensitivity per patient with seizures (focal as well as generalized seizures). The basis for the seizure yes/no assessment is the EEG.

Secondary

MeasureTime frame
Determine sensitivity per patient with seizures and simultaneously investigate drug administration, patient groups may be grouped (cluster analysis). Determine false detection rate per patient (epileptic seizure detected where none was according to EEG). Continuous comparison of the two approaches in terms of sensitivity and specificity.

Countries

Germany

Contacts

Public ContactStefan Wolking

Neurologie/ Sektion Epileptologie

swolking@ukaachen.de0049-241-80-85829

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026