UMCG
Groningen, 9715BS, Netherlands
Location status: Recruiting
NCT Number: NCT06200311
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.
Interested in participating?
Request Info65 year–80 year
All sexes
Interventional
Not applicable
Groningen, 9715BS, Netherlands
Location status: Recruiting
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Pulmonary vein isolation using pulsed field ablation (PFA), cryoballoon or radiofrequency ablation (RFA)
Other names: AF ablation
1st line: rate control, 2nd line: pharmacological rhythm management. 3rd line: AF ablation
Time frame: through study completion, a median of 2.5 years
Atrial cardiomyopathy (ACMP)-associated complications
Time frame: through study completion, a median of 2.5 years
As measured by LAVI (left atrial volume index) increase or decrease
Time frame: through study completion, a median of 2.5 years
Hospitalisations/urgent visits for AF, AFL or AT
Time frame: through study completion, a median of 2.5 years
Hospitalisations/urgent visits for heart failure
Time frame: through study completion, a median of 2.5 years
Hospitalisations/urgent visits for ischemic stroke (including TIA)
Time frame: through study completion, a median of 2.5 years
Cardiovascular death
Time frame: through study completion, a median of 2.5 years
All-cause mortality
Time frame: through study completion, a median of 2.5 years
Time frame: through study completion, a median of 2.5 years
Contact information is provided by the study sponsor or research team.
Michiel Rienstra, Prof. dr.
CONTACT
Nick L van Vreeswijk, Drs.
CONTACT
University Medical Center Groningen
Other
Acronym: RACE X
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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