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Complex Arrhythmia Registry

Complex Arrhythmia Registry(CAR): Long-term Outcomes of Catheter Ablation for Atrial Fibrillation or Ventricular Tachycardia: A Multicenter, Prospective Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07024927
Acronym
CAR
Enrollment
4000
Registered
2025-06-17
Start date
2025-10-21
Completion date
2032-06-01
Last updated
2026-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation (AF), Ventricular Tachycardia (VT)

Keywords

atrial fibrillation, ventricular tachycardia, ablation, registry study

Brief summary

This is a prospective, non-randomized, multicenter observational registry study designed to systematically evaluate the long-term efficacy and safety of catheter ablation for treating atrial fibrillation (AF) and ventricular tachycardia (VT) in Chinese patients.

Detailed description

With the advancement of cardiac electrophysiology, the latest radiofrequency ablation technologies have played a significant role in the treatment of AF and VT. However, long-term outcome data on the application of these advanced techniques in Chinese patients still remains limited. The prospective, non-randomized, multicenter observational registry study will be divided into two cohorts: 1. The AF Cohort will focus on evaluating the effectiveness and safety of different ablation workflows. It aims to redefine the relationship between AF recurrence and long-term outcomes using AF burden, thereby further optimizing treatment strategies for AF. 2. The VT Cohort will primarily assess the application effects of novel technologies in VT treatment. These data will provide critical reference information for future diagnostic and management strategies for complex arrhythmias.

Interventions

PROCEDUREAF ablation

Catheter ablation will be performed under general anesthesia or local anesthesia. Pulmonary vein isolation (PVI) was performed in all patients. Beyond this mandatory step, the specific ablation strategy/protocol and ablation parameters/settings will be determined at the discretion of the operating physicians at each participating center.

PROCEDUREVT ablation

For patients with hemodynamically stable VT, comprehensive chamber mapping (including activation mapping, substrate mapping, and entrainment mapping) is recommended. This aims to elucidate the VT activation sequence and identify the critical isthmus. Precise ablation targeting the isthmus should be performed to terminate the VT. For patients with hemodynamically unstable VT, substrate mapping during sinus rhythm can be performed first. This includes identification of low-voltage zones and abnormal electrograms (e.g., late potentials, local abnormal ventricular activities - LAVAs). Targeted substrate modification ablation should then be conducted based on the mapping findings. For all patients, complete substrate mapping is recommended after VT termination.

Sponsors

Beijing Anzhen Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Atrial Fibrillation (AF) Cohort: * Inclusion Criteria (Patients must meet ALL of the following criteria): 1. Age ≥ 18 years. 2. Diagnosed with atrial fibrillation (AF), including paroxysmal AF (PAF) and persistent AF (PsAF). 3. Scheduled to undergo first-time catheter ablation for AF. 4. Procedure to be performed using a 3D mapping system. 5. Provision of signed written informed consent for study participation and willingness and ability to comply with all protocol-required follow-up assessments. *

Exclusion criteria

(Patients meeting ANY of the following criteria will be excluded): 1. Severe congenital heart disease (e.g., Tetralogy of Fallot, corrected transposition of the great arteries). 2. AF secondary to a clearly reversible cause (e.g., hyperthyroidism, post-operative state, acute alcohol intoxication). 3. Unstable angina pectoris or acute myocardial infarction (MI) within 30 days prior to enrollment/procedure. 4. Severe active infection (e.g., septic shock, sepsis). 5. Contraindications to anticoagulation therapy. 6. Current participation in another interventional clinical trial that may confound the results of this study. 7. Any other condition where, in the investigator's judgment, the patient is unsuitable for participation in this study. 2. Ventricular Tachycardia (VT) Cohort * Inclusion Criteria (Patients must meet ALL of the following criteria): 1. Age ≥ 18 years. 2. Diagnosed with ventricular tachycardia (VT) associated with underlying structural heart disease, including: 3. Ischemic heart disease (e.g., prior MI, coronary artery disease). 4. Non-ischemic cardiomyopathy (e.g., dilated cardiomyopathy (DCM), arrhythmogenic right ventricular cardiomyopathy (ARVC), hypertrophic cardiomyopathy (HCM)). 5. Scheduled to undergo first-time catheter ablation for VT. 6. Procedure to be performed using a 3D mapping system. 7. Provision of signed written informed consent for study participation and willingness and ability to comply with all protocol-required follow-up assessments. *

Design outcomes

Primary

MeasureTime frameDescription
Freedom from any documented atrial arrhythmia in 12 months after the index ablation procedureFrom the end of the 3-month blanking period post-ablation to the 12-month follow-up
Composite outcomes of ventricular tachycardia recurrence, cardiovascular hospitalization, or death during the 12-month follow-up12 monthsRecurrent ventricular tachycardia is defined as any appropriate implantable cardiac defibrillation therapy (shock or antitachycardia pacing) or documented sustained monomorphic ventricular tachycardia \>30 seconds. Cardiovascular rehospitalization is defined as a hospital admission after the randomly assigned procedure for heart failure, procedure-associated complications, or arrhythmic causes during the 12-month follow-up.

Countries

China

Contacts

CONTACTDeyong Long, MD
dragon2008@vip.sina.com+86 (010) 84005361
CONTACTDeyong Long
dragon2008@vip.sina.com+86 (010) 84005361
PRINCIPAL_INVESTIGATORDeyong Long

Beijing Anzhen Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 5, 2026