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NCT Number: NCT06200311

Atrial Fibrillation (AF) Ablation to Prevent Disease Progression of AF-induced Atrial Cardiomyopathy in Women and Men

The goal of clinical trial is to compare AF ablation to pharmacological rhythm management (being rate or rhythm control) in AF patients with signs of atrial cardiomyopathy (as defined by left atrial volume index >34 ml/m2) The main objective it aims to answer is to determine whether AF ablation compared to pharmacological rhythm management in ACMP patients with AF reduces the incidence of the composite primary endpoint of CV death and first CV hospitalization/urgent visit.

Recruiting

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Key information

Age range

65 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UMCG

Groningen, 9715BS, Netherlands

Location status: Recruiting

About this study

The RACE X trial investigates the impact of atrial cardiomyopathy (ACMP) and ablation timing on adverse outcomes in atrial fibrillation (AF) patients. ACMP leads to an atrial substrate less responsive to rhythm control, exacerbating AF recurrence and progression. This trial assesses whether AF ablation versus pharmacological rhythm management reduces the combined primary endpoint of cardiovascular (CV) death and hospitalization in ACMP and AF patients. Secondary objectives include measuring ACMP progression, ACMP-related outcomes, mortality, hospitalizations, AF symptoms, quality of life, and healthcare costs. Exploratory goals involve various additional measurements. This prospective, multicenter, open-label, blinded-endpoint, phase IIIb trial randomizes patients with ACMP and AF to receive either AF ablation or pharmacological rhythm management. Follow-up involves mobile health (mHealth) applications, questionnaires, and heart rhythm monitoring across 13 Dutch hospitals. Ineligible patients undergoing AF ablation join an observational registry. The trial population consists of patients aged 65-80 years with confirmed ACMP and ECG-confirmed AF. With 604 patients and a median 2.5-year follow-up, the trial aims to assign patients equally to each intervention. The primary endpoint is a composite of CV death and hospitalization. Catheter ablation, a safe and efficient technique, minimizes patient burden, and remote follow-up through mHealth reduces site visits. Additional study procedures are integrated into routine care, ensuring a streamlined process.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Confirmed ACMP (LAVI >34 ml/m2)
  • ECG-confirmed AF
  • Age: 65-80 years old
  • Patients eligible for both treatment strategies judged by the treating physician signed and dated informed consent prior to admission to the trial

Exclusion criteria

  • Longstanding (>1 year) persistent or permanent (accepted) AF
  • Previous left atrial (LA) ablation or LA surgery
  • AF due to a reversible cause (e.g. hyperthyroidism, post-operative AF)
  • Recent (<90 days) acute coronary syndrome, stroke/TIA or cardiac intervention (Cardiac interventions include percutaneous coronary intervention, coronary artery bypass grafting, and heart valve repair or replacement (endovascular or surgical))
  • Intracardiac thrombus
  • HF NYHA III/IV
  • Impaired renal function, defined as estimated glomerular filtration rate ≤25 ml/min/1.73m2
  • Presence of (or scheduled for) mechanical assist device or heart transplant
  • Severe aortic or mitral valve disease
  • Complex congenital heart disease
  • Life expectancy <1 year
  • Currently enrolled in another clinical randomized trial

Treatment and study plan

pulmonary vein isolation

Procedure

Pulmonary vein isolation using pulsed field ablation (PFA), cryoballoon or radiofrequency ablation (RFA)

Other names: AF ablation

Pharmacological rhythm management

Drug

1st line: rate control, 2nd line: pharmacological rhythm management. 3rd line: AF ablation

Primary outcomes

  1. A composite of cardiovascular (CV) death and first CV hospitalisation/urgent visit.

    Time frame: through study completion, a median of 2.5 years

    Atrial cardiomyopathy (ACMP)-associated complications

Secondary outcomes

  1. ACMP progression or regression

    Time frame: through study completion, a median of 2.5 years

    As measured by LAVI (left atrial volume index) increase or decrease

  2. Hospitalisations/urgent visits for AF, atrial flutter (AFL) or atrial tachycardia (AT)

    Time frame: through study completion, a median of 2.5 years

    Hospitalisations/urgent visits for AF, AFL or AT

  3. Hospitalisations/urgent visits for heart failure (HF)

    Time frame: through study completion, a median of 2.5 years

    Hospitalisations/urgent visits for heart failure

  4. Hospitalisations/urgent visits for ischemic stroke (including transient ischemic attack (TIA))

    Time frame: through study completion, a median of 2.5 years

    Hospitalisations/urgent visits for ischemic stroke (including TIA)

  5. Cardiovascular death

    Time frame: through study completion, a median of 2.5 years

    Cardiovascular death

  6. All-cause mortality

    Time frame: through study completion, a median of 2.5 years

    All-cause mortality

  7. Symptoms and improve quality of life (QoL) measured by EuroQol-5D-5L questionnaire. (higher score indicating a better QoL)

    Time frame: through study completion, a median of 2.5 years

  8. Symptoms and improve quality of life (QoL) measured by Atrial Fibrillation Effect on Quality of Life (AFEQT) questionnaire (higher score indicating less symptoms and a better QoL)

    Time frame: through study completion, a median of 2.5 years

Study contacts

Contact information is provided by the study sponsor or research team.

Michiel Rienstra, Prof. dr.

CONTACT

[email protected]

+31503616161

Nick L van Vreeswijk, Drs.

CONTACT

[email protected]

0624678451

Sponsors and collaborators

Lead sponsor

University Medical Center Groningen

Other

Registry information

Acronym: RACE X

Important dates

Study start
2024
Primary completion
2029
Study completion
2029
First posted
Jan 11, 2024
Registry last updated
Oct 18, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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