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Atrial Fibrillation Vulnerability Assessed by Echocardiography as Predictor of Post-ablation Atrial Fibrillation Recurrence: Prospective Three-year Follow-up Study

Atrial Fibrillation Vulnerability Assessed by Echocardiography as Predictor of Post-ablation Atrial Fibrillation Recurrence: Prospective Three-year Follow-up Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-14005616
Enrollment
Unknown
Registered
2014-10-22
Start date
2015-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

atrial fibrillation

Interventions

Case series:ablation

Sponsors

Shandong University/Qilu Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Age:18-75years; 2) presence of drug-refractory symptomatic paroxysmal or persistent AF as evidenced by 12-lead electrocardiogram (ECG) and 24h Holter monitoring; 3) absence of left atrial appendage/left atrium thrombus in TEE, or coronary CT examination if TEE is not tolerated; 4) left ventricular ejection fraction more than 30%; 5) left atrial diameter less than 55mm; 6) patient undergoing RFCA; and 7) agreed to participate in this study and complete follow-up by signing informed consent.

Exclusion criteria

Exclusion criteria: 1)Severe cardiomyopathy, valvular disease, congenital heart disease, decompensated heart failure and left ventricular dysfunction; 2) malignant tumors, acute or chronic infection, hyperthyroidism, connective tissue disease, liver and kidney dysfunction, poor control of blood pressure; 3) history of acute cardiovascular and cerebrovascular events, trauma or surgery within three previous months; 4) on immunosuppressive therapy and with low numbers of white blood cells; 5) reversible atrial fibrillation caused by thyroid hyperfunction, alcohol drinking, surgery or other causes; 6) failed ablation or severe post-ablation complications; 7) patient with contraindications to anti-coagulation; 8) pregnant or breast-feeding women; or 9) participation in other clinical research.

Design outcomes

Primary

MeasureTime frame
Atrial fibrillation vulnerability;

Countries

China

Contacts

Public ContactJing-quan Zhong
gilman_zhong@hotmail.com+86 13791123056

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026