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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05638841
Other study ID # 2022-653-01
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2023
Est. completion date December 31, 2026

Study information

Verified date December 2023
Source Peking University Third Hospital
Contact Yanguang Li, Doctor
Phone +8613693327068
Email liyanguangsuper@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this study, the continuous inclusion of atrial fibrillation patients treated by catheter ablation in the Department of Cardiology, Peking University Third Hospital, through the collection of clinical data and outpatient follow-up, to explore the risk factors of atrial fibrillation recurrence after catheter ablation and the influencing factors of major clinical events in atrial fibrillation patients, and further guide the management mode of atrial fibrillation patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date December 31, 2026
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 1) Age > 18 - 2) ECG or holter electrocardiogram confirmed atrial fibrillation Exclusion Criteria: - 1) Hematological diseases, autoimmune diseases and malignant tumors - 2) Immobility caused by hemiplegia or severe trauma - 3) The expected survival time is less than 2 years - 4) Poor compliance and high risk of expected loss of follow-up - 5) Disorders of consciousness or Alzheimer's disease

Study Design


Related Conditions & MeSH terms


Intervention

Other:
After radiofrequency ablation of atrial fibrillation
This study imposed an intervention. Clinical data were obtained by telephone or outpatient follow-up.

Locations

Country Name City State
China Peking-University-Third-Hospital Beijing

Sponsors (1)

Lead Sponsor Collaborator
Peking University Third Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Compound cardiovascular event Stroke, hemorrhage, re-hospitalization for atrial fibrillation and heart failure, and all-cause death 24 months
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