About this trial
The goal of this observational study is to follow all patients implanted with extravascular implantable cardioverter-defibrillators (EV-ICDs) in Belgium throughout the lifetime of the devices. The main goal of the study is to keep track of:
* all parameters of the device * complications * arrhythmia detection and therapy delivery * clinical endpoints (quality of life, cardiac and infectious events) Participants who underwent or will undergo an EV-ICD implantation as part of their regular medical care will be asked if data can be collected from their medical record. No additional tasks are required for the study.
Eligibility criteria
Qualifiers
At least 18 years old
Previous or planned EV-ICD implantation (successful or not)
Informed consent signed
Disqualifiers
Patients who did not undergo any step of the implantation procedure
Trial design
Treatments tested in this trial
- Not listed