Artifacts and Misclassification by the Wearable Cardioverter-Defibrillator

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00030855

Enrollment

150

Registered

2022-12-15

Start date

2016-12-03

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

prevention of sudden cardiac death

Interventions

Group 1: Patients with indication for the wearable cardioverter-defibrillator

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Indication for a wearable cardioverter-defibrillator

Exclusion criteria

Exclusion criteria: 1. Age below 18 years 2. Not able to give consent / patients in permanent care

Design outcomes

Primary

Measure	Time frame
Episodes of artifacts and / or misclassifications with or without active termination of therapy by the patient	—

Secondary

Measure	Time frame
1. Episodes of ventricular arrhythmia 2. Wearing time in total and per day	—

Countries

Germany

Contacts

Public ContactFlorian Blaschke

Charité Universitätsmedizin Berlin, Campus Virchow Klinikum, Abteilung Kardiologie

florian.blaschke@charite.de+49 30 450 653 635

Outcome results

None listed

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