# The CONDUCT‐AF trial: Rationale and design of a prospective, randomized, multicentre study comparing conduction system and biventricular pacing in patients undergoing atrioventricular node ablation for heart failure with atrial fibrillation

**Authors:** Maja Ivanovski, Miha Mrak, Anja Zupan Mežnar, Matevž Jan, Catalin Pestrea, Sandro Brusich, Peter Bogyi, Sebastiaan Dhont, Zrinka Jurišić, Vassil Traykov, Borka Pezo Nikolić, Wilfried Mullens, David Žižek

PMC · DOI: 10.1002/ejhf.70013 · 2025-09-08

## TL;DR

This study compares two heart pacing methods in patients with heart failure and atrial fibrillation to see which improves heart function and outcomes better.

## Contribution

The trial introduces a novel comparison of conduction system pacing versus biventricular pacing in patients undergoing AVNA for heart failure and AF.

## Key findings

- The trial will assess whether conduction system pacing is non-inferior to biventricular pacing in improving LVEF.
- It will evaluate clinical outcomes like heart failure worsening and cardiovascular death.
- Quality of life and safety outcomes will also be analyzed over a 24-month follow-up.

## Abstract

There is a lack of data from randomized clinical trials comparing treatment outcomes between conduction system pacing (CSP) modalities and biventricular pacing (BVP) in symptomatic patients with refractory atrial fibrillation (AF) scheduled for atrioventricular node ablation (AVNA). The CONDUCT‐AF investigates whether CSP is non‐inferior to BVP in improving left ventricular ejection fraction (LVEF) and clinical outcomes in heart failure (HF) patients with symptomatic AF undergoing AVNA.

This study is an investigator‐initiated, prospective, randomized, multicentre clinical trial conducted across 10 European centres, enrolling 82 patients with symptomatic AF, HF with reduced LVEF, and narrow QRS. Participants will be randomized 1:1 to CSP or BVP with subsequent AVNA and followed for at least 24 months. The primary endpoint is the change in LVEF after 6 months. Secondary endpoints will include time to the first occurrence of worsening HF or cardiovascular death and its individual components, total number of HF hospitalizations, change in quality of life, N‐terminal pro‐B‐type natriuretic peptide, 6‐min walk test distance, and safety outcomes.

The CONDUCT‐AF trial will provide critical insights into the optimal pacing modality for patients with HF and refractory AF undergoing AVNA. Recruitment is expected to conclude in 2025, with the first study results anticipated in 2026.

## Linked entities

- **Diseases:** atrial fibrillation (MONDO:0004981), heart failure (MONDO:0005252)

## Full-text entities

- **Diseases:** cardiovascular death (MESH:D002318), HF (MESH:D006333), AF (MESH:D001281)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC12575416