World Health Organization site
Skip Navigation Links

Main
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: ChiCTR
Last refreshed on: 18 April 2017
Main ID:  ChiCTR-OOC-14005616
Date of registration: 2014-10-22
Prospective Registration: Yes
Primary sponsor: Shandong University/Qilu Hospital
Public title: Atrial Fibrillation Vulnerability Assessed by Echocardiography as Predictor of Post-ablation Atrial Fibrillation Recurrence: Prospective Three-year Follow-up Study
Scientific title: Atrial Fibrillation Vulnerability Assessed by Echocardiography as Predictor of Post-ablation Atrial Fibrillation Recurrence: Prospective Three-year Follow-up Study
Date of first enrolment: 2015-01-01
Target sample size: Case series:200;
Recruitment status: Pending
URL:  http://www.chictr.org.cn/showproj.aspx?proj=10008
Study type:  Observational study
Study design:  Case series  
Phase:  Other
Countries of recruitment
China
Contacts
Name: Jing-quan Zhong   
Address:  107 Wen Hua Xi Lu, Lixia District, Jinan, Shandong Province, China
Telephone: +86 13791123056
Email: gilman_zhong@hotmail.com
Affiliation: 
Name: Jing-quan Zhong   
Address:  107 Wen Hua Xi Lu, Lixia District, Jinan, Shandong Province, China
Telephone: +86 13791123056
Email: gilman_zhong@hotmail.com
Affiliation:  Shandong University/Qilu Hospital
Key inclusion & exclusion 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: 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
Health Condition(s) or Problem(s) studied
atrial fibrillation
Intervention(s)
Case series:ablation;
Primary Outcome(s)
Atrial fibrillation vulnerability;
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Funded by Biosense Webster
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history