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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. |
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Register:
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ChiCTR |
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Last refreshed on:
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18 April 2017 |
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Main ID: |
ChiCTR-OOC-15006130 |
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Date of registration:
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2014-10-30 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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An observational study:Relaxin levels in patients with atrial fibrillation and its relationship with atrial fibrosis
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Scientific title:
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An observational study:Relaxin levels in patients with atrial fibrillation and its relationship with atrial fibrosis |
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Date of first enrolment:
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2014-04-01 |
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Target sample size:
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AF Group :200;Control Group:200; |
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Recruitment status: |
Completed |
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URL:
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http://www.chictr.org.cn/showproj.aspx?proj=10620 |
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Study type:
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Observational study |
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Study design:
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Case-Control study
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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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Hao Zhou
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Address:
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Shangcai South village, Ouhai district, Wenzhou, Zhejiang
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Telephone:
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+86 13968801939 |
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Email:
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wyzh66@126.com |
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Affiliation:
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Name:
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Xiang Qu
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Address:
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Shangcai South village, Ouhai district, Wenzhou, Zhejiang
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Telephone:
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+86 13616633181 |
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Email:
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cookie774@163.com |
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Affiliation:
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The first hospital affiliated of wenzhou medical university |
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Key inclusion & exclusion criteria
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Inclusion criteria: 1.Patients are diagnosed by electrocardiogram as atrial fibrillation;
2.Patients provide voluntarily his/her blood samples and cooperate with treatment and check;
3.Patients are willing to review and follow-up after atrial fibrillation with radiofrequency ablation for 5 to 7 months.
Exclusion criteria: 1.Patients who eventually are diagnosed as other types of arrhythmias;
2.The acute heart failure patients need dialysis or rescue breathing machine;
3.Patients who are hemodynamic instability or myocardial infarction for killip 3-4 level need breathing machine or IABP support;
4.Patients who appear severe complications after ablation, such as injure the his bundle, II or III degree atrioventricular block and cardiac perforation;
5.Any situation that researchers consider the patient's condition will interfere is not be into the group.
Age minimum:
18
Age maximum:
80
Gender:
Both
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Health Condition(s) or Problem(s) studied
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atrial fibrillaiton
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Intervention(s)
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AF Group :Radiofrequency ablation or conservative treatment ;Control Group:None;
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Primary Outcome(s)
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Relaxin;Blood;
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Source(s) of Monetary Support
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Zhejiang province natural science fund
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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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