Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ChiCTR |
Last refreshed on:
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18 April 2017 |
Main ID: |
ChiCTR-OOC-14005616 |
Date of registration:
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2014-10-22 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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Atrial Fibrillation Vulnerability Assessed by Echocardiography as Predictor of Post-ablation Atrial Fibrillation Recurrence: Prospective Three-year Follow-up Study
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Scientific title:
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Atrial Fibrillation Vulnerability Assessed by Echocardiography as Predictor of Post-ablation Atrial Fibrillation Recurrence: Prospective Three-year Follow-up Study |
Date of first enrolment:
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2015-01-01 |
Target sample size:
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Case series:200; |
Recruitment status: |
Pending |
URL:
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http://www.chictr.org.cn/showproj.aspx?proj=10008 |
Study type:
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Observational study |
Study design:
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Case series
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Phase:
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Other
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Countries of recruitment
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China
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Contacts
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Name:
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Jing-quan Zhong
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Address:
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107 Wen Hua Xi Lu, Lixia District, Jinan, Shandong Province, China
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Telephone:
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+86 13791123056 |
Email:
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gilman_zhong@hotmail.com |
Affiliation:
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Name:
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Jing-quan Zhong
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Address:
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107 Wen Hua Xi Lu, Lixia District, Jinan, Shandong Province, China
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Telephone:
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+86 13791123056 |
Email:
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gilman_zhong@hotmail.com |
Affiliation:
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Shandong University/Qilu Hospital |
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Key inclusion & exclusion criteria
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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: 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.
Age minimum:
18
Age maximum:
75
Gender:
Both
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Health Condition(s) or Problem(s) studied
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atrial fibrillation
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Intervention(s)
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Case series:ablation;
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Primary Outcome(s)
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Atrial fibrillation vulnerability;
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Source(s) of Monetary Support
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Funded by Biosense Webster
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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