Danish Evaluation of Early Catheter Ablation for Atrial Fibrillation in Patients With Heart Failure

NCT06560047 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1616

Last updated 2024-08-30

No results posted yet for this study

Summary

The DanAblate-HF trial will investigate whether early catheter ablation treatment for atrial fibrillation in patients with heart failure is superior to standard treatment.

Conditions

Interventions

PROCEDURE

Catheter ablation

Catheter ablation with pulmonary vein isolation will be the study intervention. Patients randomized to the intervention arm will undergo catheter ablation within six weeks of randomization. In the waiting-time for ablation, patients will receive standard treatment for AF and HF, as per current guideline recommendations. Catheter ablation will be performed at one of six high-volume ablation centers in Denmark. Mode of catheter ablation will be at the discretion of the operator. Radiofrequency ablation, cryo-balloon ablation and pulsed-field ablation will be utilized. The treating physician should ensure successful pulmonary vein isolation after ablation with either post-procedural mapping or pacing, as per current standards. Only pulmonary vein isolation will be performed during the ablation procedure.

Sponsors & Collaborators

  • Rigshospitalet, Denmark

    collaborator OTHER
  • Odense University Hospital

    collaborator OTHER
  • Aarhus University Hospital

    collaborator OTHER
  • Zealand University Hospital

    collaborator OTHER
  • Herlev and Gentofte Hospital

    collaborator OTHER
  • Aalborg University Hospital

    lead OTHER

Principal Investigators

  • Sam Riahi, MD, PhD · Department of Cardiology, Aalborg Univeristy Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-08-28
Primary Completion
2029-08-31
Completion
2039-08-31

Countries

  • Denmark

Study Locations

More Related Trials

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 NCT06560047 on ClinicalTrials.gov