房颤射频消融联合左心耳封堵的有效性和安全性研究

注册号:

Registration number:

ChiCTR-OOC-17011530 

最近更新日期:

Date of Last Refreshed on:

2017-05-31 20:21:31 

注册时间:

Date of Registration:

2017-05-31 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

房颤射频消融联合左心耳封堵的有效性和安全性研究

Public title:

Efficacy and safety of Combined Catheter Ablation for AF and LAA Occlusion procedures

注册题目简写:

English Acronym:

研究课题的正式科学名称:

房颤射频消融联合左心耳封堵的有效性和安全性研究

Scientific title:

Efficacy and safety of Combined Catheter Ablation for AF and LAA Occlusion procedures

研究课题代号(代码):

Study subject ID:

在二级注册机构或其它机构的注册号:

The registration number of the Partner Registry or other register:

申请注册联系人:

王云鹤 

研究负责人:

蒋晨阳 

Applicant:

Yunhe Wang 

Study leader:

Chenyang Jiang 

申请注册联系人电话:

Applicant telephone:

+86 13732252457

研究负责人电话:

Study leader's
telephone:

+86 13857190051

申请注册联系人传真 :

Applicant Fax:

研究负责人传真:

Study leader's fax:

申请注册联系人电子邮件:

Applicant E-mail:

yunhewang@hotmail.com

研究负责人电子邮件:

Study leader's E-mail:

jiangchenyangmail@163.com

申请单位网址(自愿提供):

Applicant website(voluntary supply):

研究负责人网址(自愿提供):

Study leader's website(voluntary supply):

申请注册联系人通讯地址:

浙江杭州庆春东路3号浙江大学医学院附属邵逸夫医院

研究负责人通讯地址:

浙江杭州庆春东路3号浙江大学医学院附属邵逸夫医院

Applicant address:

Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, 3 East Qingchun Road, Hangzhou, Zhejiang, China

Study leader's address:

Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, 3 East Qingchun Road, Hangzhou, Zhejiang, China

申请注册联系人邮政编码:

Applicant postcode:

研究负责人邮政编码:

Study leader's postcode:

申请人所在单位:

浙江大学医学院附属邵逸夫医院

Applicant's institution:

Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University

研究负责人所在单位:

浙江大学医学院附属邵逸夫医院

Affiliation of the Leader:

Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

20170327-3

伦理委员会批件附件:

Approved file of Ethical Committee:

批准本研究的伦理委员会名称:

浙江大学医学院附属邵逸夫医院伦理委员会

Name of the ethic committee:

Ethics Committee, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University

伦理委员会批准日期:

Date of approved by ethic committee:

1990-01-01 00:00:00

伦理委员会联系人:

Contact Name of the ethic committee:

伦理委员会联系地址:

Contact Address of the ethic committee:

伦理委员会联系人电话:

Contact phone of the ethic committee:

伦理委员会联系人邮箱:

Contact email of the ethic committee:

研究实施负责(组长)单位:

浙江大学医学院附属邵逸夫医院

Primary sponsor:

Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University

研究实施负责(组长)单位地址:

浙江杭州庆春东路3号

Primary sponsor's address:

3 East Qingchun Road, Hangzhou, Zhejiang, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

浙江

市(区县):

Country:

China

Province:

Zhejiang

City:

单位(医院):

浙江大学医学院附属邵逸夫医院

具体地址:

浙江杭州庆春东路3号

Institution
hospital:

Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University

Address:

3 East Qingchun Road, Hangzhou, Zhejiang, China

经费或物资来源:

圣犹达医疗用品(上海)有限公司

Source(s) of funding:

St. Jude Medical (Shanghai) Co., Ltd.

研究疾病:

心房纤维性颤动(心房纤颤)  

Target disease:

Atrial fibrillation

研究疾病代码:

I48.X04

Target disease code:

I48.X04

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

单臂 

Study design:

Single arm 

研究目的:

评价房颤消融+左心耳封堵联合术式的有效性和安全性。  

Objectives of Study:

Evaluate the efficacy and safety of the combined atrial fibrillation catheter ablation and left atrial appendage occlusion procedure.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

排除标准:

既往有左房导管消融或外科消融术史
结构性心脏病,包括先天性心脏病、心脏瓣膜疾病(中度以上,或金属瓣置换术后)、肥厚性心肌病
有可逆性病因的房颤患者,例如但不仅限于:甲状腺功能亢进
3个月内发生心肌梗死的患者
对肝素、低分子肝素、口服抗凝剂使用禁忌
经胸心超提示左心房前后径≥55mm
无论任何已知的情况,预期寿命≤2 年的患者
肝肾功能不全,跌倒高危人群,服药依从性差
症状性颈动脉疾病
合并房颤以外需抗凝治疗疾病
证实心房内血栓,肿瘤,或其他可能妨碍导管放置的疾病

Exclusion criteria:

1. Have a history of left atrial catheter ablation or surgical ablation;
2. Structural heart disease, including congenital heart disease, cardiac valve disease (moderate or severe, or prior metallic prosthetic heart valve replacement), hypertrophic cardiomyopathy;
3. Reversible causes of AF including but not limited to hyperthyroidism;
4. Myocardial infarction within 3 months prior to enrollment;
5. Patient has contra-indication to oral anticoagulation, heparin or low molecular weight heparins;
6. Left atrial diameter ≥ 60 mm (2D echocardiography, parasternal long axis view);
7. Life expectancy ≤ 2 years due to all kinds of reasons;
8. Abnormal liver or renal function;
9. High risk of accidental falls;
10. Low Treatment compliance;
11. Symptomatic carotid artery disease;
12. Need long term anticoagulation for reasons other than atrial fibrillation;
13. Proved to have thrombus, tumor or other disease that might affect the catheter placement in the atrium.

研究实施时间:

Study execute time:

From 2017-06-01 00:00:00 To 2018-12-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2017-06-01 00:00:00 To 2017-12-01 00:00:00

干预措施:

Interventions:

组别:

1

样本量:

120

Group:

1

Sample size:

干预措施:

行房颤射频消融联合左心耳封堵术

干预措施代码:

Intervention:

Combined atrial fibrillation catheter ablation and left atrial appendage occlusion procedure

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

浙江 

市(区县):

 

Country:

China

Province:

Zhejiang

City:

单位(医院):

浙江大学医学院附属邵逸夫医院 

单位级别:

三级甲等 

Institution
hospital:

Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University

Level of the institution:

Tertiary A hospital

国家:

中国

省(直辖市):

广东 

市(区县):

 

Country:

China

Province:

Guangdong

City:

单位(医院):

广东省人民医院 

单位级别:

三级甲等 

Institution
hospital:

Guangdong General Hospital

Level of the institution:

Tertiary A hospital

国家:

中国

省(直辖市):

江苏 

市(区县):

 

Country:

China

Province:

Jiangsu

City:

单位(医院):

江苏省人民医院 

单位级别:

三级甲等 

Institution
hospital:

Jiangsu Province Hospital

Level of the institution:

T

国家:

中国

省(直辖市):

四川 

市(区县):

 

Country:

China

Province:

Sichan

City:

单位(医院):

四川大学华西医院 

单位级别:

三级甲等 

Institution
hospital:

West China Hospital, Sichuan University

Level of the institution:

Tertiary A hospital

国家:

中国

省(直辖市):

浙江 

市(区县):

 

Country:

China

Province:

Zhejiang

City:

单位(医院):

宁波市第一医院 

单位级别:

三级甲等 

Institution
hospital:

Ningbo First Hospital

Level of the institution:

Tertiary A hospital

测量指标:

Outcomes:

指标中文名:

术后1年内全因死亡率

指标类型:

主要指标

Outcome:

1-year all-cause mortality post procedure

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术后1年内缺血性卒中发生率

指标类型:

主要指标

Outcome:

1-year ischemic stroke rate post procedure

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术后1年内全身栓塞发生率

指标类型:

主要指标

Outcome:

1-year systemic embolism rate post procedure

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术后1年内出血发生率

指标类型:

次要指标

Outcome:

The occurrence of bleeding in 1 year post procedure

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术后3-12月间,无抗心律失常药物情况下(β受体阻滞剂除外),无房颤/房扑/房速发作复发(有心电图证实的)生存时间

指标类型:

次要指标

Outcome:

The time free from any AF/AT (ECG confirmed) without AADs (except for β blockers) between the 3rd month to the 12th month post procedure

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

血液

组织:

Sample Name:

Blood

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

征募研究对象情况:

Recruiting status:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 65 years
最大 Max age 85 years

性别:

男女均可

Gender:

Both

随机方法(请说明由何人用什么方法产生随机序列):

N/A

Randomization Procedure (please state who generates the random number sequence and by what method):

N/A

是否公开试验完成后的统计结果:

Calculated Results after the Study Completed public access:

公开/Public

盲法:

Blinding:

试验完成后的统计结果(上传文件):

Calculated Results after
the Study Completed(upload file):

是否共享原始数据:

IPD sharing

是Yes

共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址):

将通过ResMan临床试验公共管理平台共享原始数据(http://www.medresman.org)

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

Will share IPD via Resman (http://www.medresman.org)

数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC:

使用纸质病例记录表及本地电子数据库(Excel表格)保存数据。

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

Via CRF and excel form.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

注册人:

Name of Registration:

 2017-05-31 20:21:31