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

NCT06324682 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 8400

Last updated 2024-03-22

No results posted yet for this study

Summary

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.

Conditions

  • Arrhythmias, Cardiac
  • Atrioventricular Block
  • Reduced Systolic Function
  • Atrial Fibrillation
  • Bradyarrhythmia
  • Ventricular Tachycardia
  • Ventricular Dysfunction
  • Ventricular Fibrillation
  • Ventricular Arrythmia
  • Atrioventricular Nodal Disease
  • Atrioventricular Conduction Defects
  • Atrioventricular Block Complete
  • Atrioventricular Block Incomplete
  • Atrioventricular Junctional Rhythm
  • Bundle-Branch Block
  • Left Bundle-Branch Block
  • Heart Failure, Systolic
  • Block;Atrioventricular
  • Block; Arrhythmic
  • Block; Mobitz
  • Block, Heart
  • Block, Fascicular
  • Block Branch Bundle Left
  • Heart Failure,Congestive
  • Heart Arrhythmia

Interventions

DEVICE

Cardiac pacing - Conventional RV pacing

Implantation of devices for cardiac pacing/defibrillation

DEVICE

Cardiac pacing - Conduction System Pacing

Implantation of devices for cardiac pacing/defibrillation

DEVICE

Cardiac pacing - Cardiac resynchronization therapy (pacing - CRTP - or defibrillation - CRTD)

Implantation of devices for cardiac pacing/defibrillation

DEVICE

Cardiac pacing - Epicardial pacing

Implantation of devices for cardiac pacing/defibrillation

DEVICE

Cardiac pacing - Leadless pacing

Implantation of devices for cardiac pacing/defibrillation

Sponsors & Collaborators

  • University Hospital of Ferrara

    lead OTHER

Principal Investigators

  • Matteo Bertini, MD, PhD · Azienda Ospedaliero Universitaria di Ferrara

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-01
Primary Completion
2033-12-31
Completion
2034-12-31

Countries

  • Italy

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06324682 on ClinicalTrials.gov