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Clinical Trial 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).


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05966675
Study type Interventional
Source Medical University of Silesia
Contact Krzysztof S. Golba, MD PhD
Phone +48 (32)359-88-93
Email krzysztof.golba@gmail.com
Status Not yet recruiting
Phase N/A
Start date October 1, 2023
Completion date June 2028