Cryoballoon Ablation Versus Medical Therapy in Patients With Heart Failure and Atrial Fibrillation (RACE-8-HF)

Maastricht University

Status

Terminated

Conditions

Atrial Fibrillation

Heart Failure, Systolic

Heart Failure With Reduced Ejection Fraction

Heart Failure

Treatments

Procedure: Cryoballoon ablation

Study type

Interventional

Funder types

Other

Identifiers

NCT04342832

NL71710.068.19

Details and patient eligibility

About

Rationale:

Atrial fibrillation (AF) and heart failure (HF) can cause each other and sustain each other. Combined, the two diseases negatively influence each other's prognosis and lead to higher mortality. Studies in HF patients in which the AF burden is reduced by AF ablation show promising results toward improved prognosis, but so far only one randomized trial is conducted that focused on major clinical endpoints. As the selected patients in this trial were not representative for the entire population and its ablation method varied from patient to patient, it is the aim of the present study to confirm that early invasive therapy consisting of a strict pulmonary vein isolation (PVI) protocol using cryoballoon therapy has positive effects on hard clinical endpoints in a wider variety of patients in the HF population.

Furthermore, there are no studies which compare cost-effectiveness of an early invasive strategy in this patient category. The investigators expect that avoided hospitalizations and healthcare resource utilizations lead to lower costs in the AF ablation group, despite initial higher costs of the procedure.

Objective:

To compare outcome and cost-effectiveness of early AF ablation by PVI using cryoballoon therapy with standard (medical) therapy in patients with heart failure with reduced ejection fraction.

Study design:

Multicenter, randomized, open label clinical trial.

Study population:

Symptomatic adult patients with heart failure with reduced ejection fraction (<40%) and paroxysmal or persistent AF.

Intervention:

AF ablation (PVI) using cryoballoon therapy.

Outcome measures:

The primary endpoint is a combined endpoint of all-cause mortality, unplanned cardiovascular hospitalization, and stroke (time-to-event analysis).

Secondary endpoints of the trial are:

A combined endpoint of mortality, number of unplanned cardiovascular hospitalizations, and stroke (recurrent-event analysis);
A hierarchical endpoint of mortality, unplanned cardiovascular hospitalizations, stroke, and HF complaints;
Cost-effectiveness. Key exploratory endpoints include individual components of the combined endpoints, days alive out of the hospital, hospitalizations for heart failure, recurrence of atrial arrhythmia, and quality of life.

Enrollment

64 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients aged 18-80;
HF with ejection fraction <40%, as assessed by recent (<6 months) echocardiography or cardiovascular magnetic resonance imaging (CMR);
AF, documented on standard ECG or Holter monitoring;
Eligible for both treatment arms;
Signed and dated informed consent prior to admission to the trial.

Exclusion criteria

End-stage heart failure: NYHA class IV, patients on waiting list for cardiac transplant and/or left ventricular assist device;
Long-standing (> 1 year) persistent or permanent AF;
Previous pulmonary vein isolation or surgical ablation;
Left atrial diameter ≥60 mm or left atrial volume index ≥50 ml/m2;
Impaired renal function, defined as estimated glomerular filtration rate (eGFR) ≤25 ml/min/1.73m2;
Recent (<90 days) acute coronary syndrome, cardiac intervention1, or stroke/transient ischemic attack (TIA);
Planned or expected cardiac surgery in the following year;
Active infectious disease or malignancy;
Women who are pregnant or planning to become pregnant during the trial;
Contraindication for cryoballoon ablation or other condition that may prevent subjects from adhering to the trial protocol, in the opinion of the investigator.