Recruiting NCT06388382
Investigation of the Audible ICD Alert Tone
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Alert tone demonstration.
- Who it may be relevant to
- Registry conditions: Implantable Defibrillator User. Basic parameters: 15 years — 100 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Germany
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Investigation of the Audible Alert Tone in ICD Patients with Subcutaneous Cardioverter Defibrillators
Overview
Ability of ICD patients to hear the audible ICD alert is being assessed.
Interventions
- Other Alert tone demonstration
Patients are demonstrated the alert tone of their ICD
Primary outcome measures
- Alert tone audible [Time frame: 1 minute after demonstration]
Eligibility criteria
Inclusion criteria
- patient equipped with a subcutaneous ICD
- willing to participate
Exclusion criteria
- S-ICD implantation within the past 3 weeks
- patient is deaf
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Germany · 1 center
- University Hospital Cologne — Cologne
Identifiers
NCT: NCT06388382 · UKKx2024