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

Treatment groups

8,400 Participants
are divided into 5 treatment groups

Locations

31
Azienda Ospedaliero-Universitaria di Ferrara44124, FerraraFE, Italy
Ospedale San Donato Arezzo Italy
Azienda Ospedaliero-Universitaria S.Orsola-Malpighi Bologna40138, Bologna Italy
spedale Maggiore di Bologna Bologna Italy

Sponsors and collaborators

University Hospital of Ferrara

Lead sponsor