About this trial
The goal of this observational study is to evaluate the clinical characteristics of patients undergoing permanent cardiac pacing and to compare procedural efficacy and safety of different implantation approaches in the clinical practice of the participating centres. The contribution of non-fluoroscopic anatomical and electrophysiological reconstruction systems to device implantation procedures will also be evaluated.
Participants \[patients over 18 years old with an indication to receive a definitive pacemaker/intracardiac defibrillator implant\] will receive a permanent cardiac pacing implant as requested according to European Society of Cardiology (ESC) guidelines; the investigators will evaluate procedural efficacy and safety of different implantation approaches.
Eligibility criteria
Qualifiers
Indication for cardiac stimulation
Having performed the implantation of a device for cardiac stimulation
Disqualifiers
Age < 18 years;
Pregnancy status;
Trial design
Treatments tested in this trial
- Cardiac pacing - Conventional RV pacing
- Cardiac pacing - Conduction System Pacing
- Cardiac pacing - Cardiac resynchronization therapy (pacing - CRTP - or defibrillation - CRTD)
- Cardiac pacing - Epicardial pacing
- Cardiac pacing - Leadless pacing