ConTempoRary Cardiac Stimulation in Clinical practicE: lEft, BivEntriculAr, Right, and conDuction System Pacing

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital of Ferrara

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

Sponsors and collaborators