Physiologic Cardiac Pacing to Prevent Left Ventricular Dysfunction Post Transcatheter Aortic Valve Implantation
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Atrioventricular Block, Second and Third Degree
- Sponsor
- Medical University of Silesia
- Enrollment
- 500
- Locations
- 1
- Primary Endpoint
- Heart Failure Hospitalization
- Status
- Recruiting
- Last Updated
- 10 months ago
Overview
Brief Summary
The study aims to compare permanent Conduction System Pacing (CSP) with the standard therapy - Right Ventricular Pacing (RVP) or Biventricular Pacing (BVP) - in preventing the development and progression of symptomatic Chronic Heart Failure (CHF) and improving survival in patients after Transcatheter Aortic Valve Implantation (TAVI).
Detailed Description
A multicenter randomized controlled head-to-head trial was planned to compare the effects of permanent pacemaker implantation (PPMI) using CSP (study intervention) with currently standard therapy - RVP or BVP (control group). The study population will consist of patients hospitalized after TAVI complicated with high-degree persistent atrioventricular (AV) block or newly developed complex AV or intraventricular conduction disturbances, qualified for PPMI within 30 days after surgery, following the 2021 European Society of Cardiology (ESC) guidelines on cardiac pacing and cardiac resynchronization therapy.
Investigators
Eligibility Criteria
Inclusion Criteria
- •transcatheter aortic valve implantation (TAVI) in up to 30 days before qualification to pacemaker implantation
- •Fulfilled criteria for permanent pacemaker implantation according do 2021 ESC guidelines
- •Written informed consent
- •Age of at least 18 years
Exclusion Criteria
- •Permanent pacemaker implantation before TAVI procedure
- •The occurrence of conduction disturbances more than 30 days after TAVI procedure
- •No written informed consent
- •Inability to obtain informed consent from participant
- •Predicted inability to obtain cooperation from patient during observation period
Outcomes
Primary Outcomes
Heart Failure Hospitalization
Time Frame: 12 months
Hospitalization due to heart failure as a main reason
All-cause death
Time Frame: 12 months
Death from any cause
Secondary Outcomes
- Pacing-Induced Cardiomyopathy (PICM)(24 months)
- Change in global longitudinal strain (GLS)(24 months)
- Change in the concentration of the N-terminal pro-brain natriuretic peptide (NT-proBNP)(24 months)
- Change in Quality of Life(24 months)
- Atrial Fibrillation (AF) episodes(24 months)
- Change in exercise capacity(24 months)
- Response to Cardiac Resynchronization Therapy (CRT)(24 months)
- Atrial High Rate Episodes (AHRE) in pacemaker recordings(24 months)