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Recruiting Observational

Atrial Fibrillation Patients Treated With Catheter Ablation

NCT05266144 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2020-09-04
Last updated
2025-06-05

Condition(s) studied

Atrial FibrillationAtrial Fibrillation Recurrent

Investigational drug(s) / intervention(s)

radiofrequency ablation

radiofrequency ablation: Bilateral pulmonary vein isolation, a kind of radiofrequency ablation, is performed in atrial fibrillation patients for atrial arrhythmia therapy.

Study summary

This is a single-center prospective observational cohort study of atrial fibrillation patients treated with radiofrequency ablation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Non-valvular atrial fibrillation, including paroxysmal atrial fibrillation and persistent atrial fibrillation * 18-80 years old * The anteroposterior diameter of the left atrium is less than 50mm via TTE * Patient meets the intervention criteria for bilateral pulmonary vein isolation after evaluation by electrophysiological specialists * Patient consents to ablation treatment Exclusion Criteria: * Intra-atrial thrombus detected by TEE * Hyperthyroidism * Previous radiofrequency ablation for atrial fibrillation

Primary outcome measure(s)

  • Recurrence assessed by ECG, Holter reports and outpatient physicians — at 1-year follow-up after ablation
    Recurrence includes atrial fibrillation and atrial flutter. Recurrence features including pattern, duration, burden, etc. will be recorded.
  • All-cause mortality assessed by telephone follow-up or medical records — at 1-year follow-up after ablation
    Time and cause of death will be recorded.

Trial sites (1)

FacilityCityRegionStatus
Peking Union Medical College Hospital Beijing Beijing Municipality Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05266144 on ClinicalTrials.gov ↗ ← All trials in China