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First-time Ablation of Atrial Fibrillation Registry (DIPE)

M

Medical University of Warsaw

Status

Enrolling

Conditions

Arrhythmia
Atrial Fibrillation

Treatments

Diagnostic Test: Blood-derived biomarker analysis
Diagnostic Test: Rotational angiography with three-dimensional reconstruction
Diagnostic Test: PPG-based remote heart rhythm/rate monitoring
Diagnostic Test: Mobile health-based spirometry
Diagnostic Test: ECG-based remote heart rhythm/rate monitoring
Diagnostic Test: Liver ultrasound examination
Diagnostic Test: Transthoracic and transesophageal echocardiography examination

Study type

Observational

Funder types

Other

Identifiers

NCT06381245
KB/265/2023

Details and patient eligibility

About

Atrial fibrillation (AF) is a prevalent cardiac arrhythmia affecting millions globally, with projections indicating a doubling of cases by 2050. AF is linked to heightened cardiovascular risks like stroke and increased healthcare costs. Ablation, targeting the arrhythmia substrate, is a method to manage AF, yet recurrence rates remain high (20-45% in the first year). Studies highlight the impact of comorbidities, AF characteristics, ablation techniques, and myocardial remodeling markers on AF progression and ablation efficacy. However, there's no definitive guidance on selecting these factors for predicting treatment success.

The aim of this study is to investigate predictors of successful AF ablation in the following areas: (a) clinical factors, (b) electrophysiological, (c) electrocardiographic, (d) ultrasound, (e) cardiac anatomy, (f) biomarkers.

Full description

AF is a multifactorial disease influenced by many possible mechanisms. This study will examine several different predictors of successful AF ablation: (a) clinical factors, (b) electrophysiological, (c) electrocardiographic, (d) ultrasound, (e) cardiac anatomy, (f) biomarkers. Analysis of these factors will help determine the optimal combination of predictors of successful ablation. This combination of prognostic factors can then be used to tailor therapeutic decisions specifically to individual patients and to improve patient selection for invasive treatment. Better patient selection and choice of ablation type can help increase success rates and avoid unnecessary procedures and their associated risks.

Enrollment

400 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • paroxysmal or persistent AF
  • first-time ablation of AF

Exclusion criteria

  • patients unable to give informed consent
  • serious health condition existing before ablation

Trial contacts and locations

1

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Central trial contact

Monika Gawałko, MD, PhD

Data sourced from clinicaltrials.gov

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