EligibleTrials
Conditions › Heart failure › NCT06324682

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

Recruiting · NCT06324682 · Observational (researchers observe without assigning treatment) · Lead sponsor: University Hospital of Ferrara

View the official record on ClinicalTrials.gov →
Heart failureAtrial Fibrillation

Interventions studied

Cardiac pacing - Cardiac resynchronization therapy (pacing - CRTP - or defibrillation - CRTD)Cardiac pacing - Conduction System PacingCardiac pacing - Conventional RV pacingCardiac pacing - Epicardial pacingCardiac pacing - Leadless pacing

What this trial is about

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.

Who can take part

Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)

Inclusion criteria

Exclusion criteria

Where it is running

31 locations listed.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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