Clinical Trials in China / NCT05266144
Recruiting
Observational
Atrial Fibrillation Patients Treated With Catheter Ablation
NCT05266144 · tracked via the Priya Life Science China tracker
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| Peking Union Medical College Hospital | Beijing | Beijing Municipality | Recruiting |
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Other trials for the same condition
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