ChiCTR2000033624 版本V1.4 版本创建时间2020/06/07 10:55:25 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2000033624 

最近更新日期:

Date of Last Refreshed on:

2020-06-07 10:52:29 

注册时间:

Date of Registration:

2020-06-07 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

心腔内超声指导下 “极低射线”导管消融治疗阵发性心房颤动的有效性和安全性研究:一项非劣效、多中心、前瞻性随机对照研究(PAF-ICE研究)

Public title:

The efficacy and safety of IntraCardiac Echocardiography (ICE)-guided minimized fluoroscopy ablation in patients with Paroxysmal Atrial Fibrillation (PAF): A Non-inferior, Multi-center, Prospective Randomized Trial (PAF-ICE trial)

注册题目简写:

PAF-ICE研究

English Acronym:

PAF-ICE trial

研究课题的正式科学名称:

心腔内超声指导下 “极低射线”导管消融治疗阵发性心房颤动的有效性和安全性研究:一项非劣效、多中心、前瞻性随机对照研究(PAF-ICE研究)

Scientific title:

The efficacy and safety of IntraCardiac Echocardiography (ICE)-guided minimized fluoroscopy ablation in patients with Paroxysmal Atrial Fibrillation (PAF): A Non-inferior, Multi-center, Prospective Randomized Trial (PAF-ICE trial)

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:

蒋汝红 

研究负责人:

蒋晨阳 

Applicant:

Ruhong Jiang 

Study leader:

Chenyang Jiang 

申请注册联系人电话:

Applicant telephone:

+86 13588425208

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:

jrh@zju.edu.cn

研究负责人电子邮件:

Study leader's E-mail:

cyjiang@zju.edu.cn

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:

浙江省杭州市庆春东路3号

研究负责人通讯地址:

浙江省杭州市庆春东路3号

Applicant address:

3 East Qingchun Road, Hangzhou, Zhejiang, China

Study leader's address:

3 East Qingchun Road, Hangzhou, Zhejiang, China

申请注册联系人邮政编码:

Applicant postcode:

310016

研究负责人邮政编码:

Study leader's postcode:

310016

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, School 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, School of Medicine, Zhejiang University

是否获伦理委员会批准:

是/Yes

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

20200512-12

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件View

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医学伦理委员会

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:

2020-05-22 00:00:00

伦理委员会联系人:

方滢芝

Contact Name of the ethic committee:

Yingzhi Fang

伦理委员会联系地址:

浙江省杭州市庆春东路3号

Contact Address of the ethic committee:

3 East Qingchun Road, Hangzhou, Zhejiang, China

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, School of Medicine, Zhejiang University

研究实施负责(组长)单位地址:

浙江省杭州市庆春东路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):

杭州

Country:

China

Province:

Zhejiang

City:

Hangzhou

单位(医院):

邵逸夫医院

具体地址:

浙江省杭州市庆春东路3号

Institution
hospital:

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

Address:

3 East Qingchun Road, Hangzhou, Zhejiang

经费或物资来源:

Biosense Webster,Inc., 3333 Diamond Canyon Road, Diamond Bar, CA, US

Source(s) of funding:

Biosense Webster,Inc., 3333 Diamond Canyon Road, Diamond Bar, CA, US

Target disease:

Atrial fibrillation

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

病例对照研究 

Study design:

Case-Control study 

研究目的:

比较ICE指导下 “极低射线”导管消融和无ICE指导常规导管消融治疗阵发性心房颤动的有效性和安全性  

Objectives of Study:

To compare the efficacy and safety of ICE-guided minimized fluoroscopy ablation and ablation without ICE in patients with paroxysmal AF

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

1)年龄:18-75岁
2)症状性阵发性房颤
3)消融手术前6个月内至少有一份心电图记录证实房颤
4)第1次行房颤导管消融术
5)患者签署知情同意书并能够完成术后随访

Inclusion criteria

1. Aged 18-75 years;
2. Symptomatic paroxysmal AF;
3. At least one electrocardiographically documented AF within 6 months of the ablation procedure;
4. First catheter ablation;
5. Patient is able and willing to provide written informed consent and complete the follow-up.

排除标准:

1)3个月内有心肌梗死,冠脉搭桥或支架植入病史
2)左心房前后径 >50mm
3)心超提示左室射血分数<40%
4)NYHA心功能分级III级或IV级
5)既往有心脏外科手术病史或房颤消融病史
6)左心房内血栓形成或肿瘤
7)严重心脏瓣膜疾病
8)存在可逆性房颤病因,如甲亢、低钾血症等
9)不能耐受抗凝治疗
10)孕妇或哺乳期女性

Exclusion criteria:

1. Myocardial infarction, CABG or PCI within preceding 3 months;
2. Left atrial diameter >50mm;
3. Left ventricular ejection fraction by echocardiography <40%;
4. NYHA class III or IV or decompensated heart failure;
5. History of cardiac surgery or any previous ablation for AF;
6. Intracardiac thrombus or tumor;
7. Severe valvular heart disease;
8. Secondary atrial fibrillation, i.e. hyperthyroidism, hypokalemia, etc.;
9. Contradictions to anticoagulation;
10. Females who are pregnant or breast feeding.

研究实施时间:

Study execute time:

From 2020-06-08 00:00:00 To 2023-06-07 00:00:00  

征募观察对象时间:

Recruiting time:

From 2020-06-08 00:00:00 To 2021-06-07 00:00:00  

干预措施:

Interventions:

组别:

ICE指导下极低射线消融组

样本量:

194

Group:

ICE-guided Minimized fluoroscopy group

Sample size:

干预措施:

ICE指导下房颤消融

干预措施代码:

Intervention:

ICE-guided AF ablation

Intervention code:

组别:

无ICE常规消融组

样本量:

194

Group:

Tradional group without ICE

Sample size:

干预措施:

无ICE指导常规房颤消融

干预措施代码:

Intervention:

Tradional AF ablation without ICE

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):

杭州 

Country:

China 

Province:

Zhejiang 

City:

Hangzhou 

单位(医院):

浙江大学医学院附属邵逸夫医院 

单位级别:

三甲医院 

Institution
hospital:

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

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

云南 

市(区县):

 

Country:

China 

Province:

Yunnan 

City:

 

单位(医院):

云南省第一人民医院 

单位级别:

三甲 

Institution
hospital:

The First People's Hospitalof Yunnan Province

Level of the institution:

Tertiary A

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:

三甲 

Institution
hospital:

JiangSu Province Hospital

Level of the institution:

Tertiary A

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:

三甲 

Institution
hospital:

Guangdong Provincial People's Hospital

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

广东 

市(区县):

 

Country:

China 

Province:

Guangdong 

City:

 

单位(医院):

南方医院 

单位级别:

三甲 

Institution
hospital:

Nanfang Hospital

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

北京 

市(区县):

 

Country:

China 

Province:

Beijing 

City:

 

单位(医院):

首都医科大学附属北京朝阳医院 

单位级别:

三甲 

Institution
hospital:

Beijing Chao-Yang Hospital, Capital medical University

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

浙江 

市(区县):

 

Country:

China 

Province:

Zhejiang 

City:

 

单位(医院):

温州医科大学附属第一医院 

单位级别:

三甲 

Institution
hospital:

The First Affiliated Hospital of Wenzhou Medical University

Level of the institution:

Teritary A

国家:

中国

省(直辖市):

浙江 

市(区县):

 

Country:

China 

Province:

Zhejiang 

City:

 

单位(医院):

温州医科大学附属第二医院 

单位级别:

三甲 

Institution
hospital:

The Second Affiliated Hospital of Wenzhou Medical University

Level of the institution:

Teritary A

国家:

中国

省(直辖市):

北京 

市(区县):

 

Country:

China 

Province:

Beijing 

City:

 

单位(医院):

北京大学人民医院 

单位级别:

三甲 

Institution
hospital:

Peking University People's Hospital

Level of the institution:

Teritary A

国家:

中国

省(直辖市):

浙江 

市(区县):

 

Country:

China 

Province:

Zhejiang 

City:

 

单位(医院):

台州医院 

单位级别:

三甲 

Institution
hospital:

Taizhou Hospital

Level of the institution:

Teritary A

国家:

中国

省(直辖市):

河北 

市(区县):

 

Country:

China 

Province:

Hebei 

City:

 

单位(医院):

河北医科大学第二医院 

单位级别:

三甲 

Institution
hospital:

The second hospital of Heibei Medical University

Level of the institution:

Teritary A

国家:

中国

省(直辖市):

四川 

市(区县):

 

Country:

China 

Province:

Sichuan 

City:

 

单位(医院):

四川省人民医院 

单位级别:

三甲 

Institution
hospital:

Sichuan Provincial People’s Hospital

Level of the institution:

Teritary A

国家:

中国

省(直辖市):

安徽 

市(区县):

 

Country:

China 

Province:

Anhui 

City:

 

单位(医院):

安徽医科大学第一附属医院 

单位级别:

三甲 

Institution
hospital:

The First Affiliated Hospital of Medical University Of Anhui

Level of the institution:

Teritary A

国家:

中国

省(直辖市):

广东 

市(区县):

 

Country:

China 

Province:

Guangdong 

City:

 

单位(医院):

珠江医院 

单位级别:

三甲 

Institution
hospital:

Zhujiang Hospital

Level of the institution:

Teritary A

国家:

中国

省(直辖市):

山西 

市(区县):

 

Country:

China 

Province:

Shanxi 

City:

 

单位(医院):

山西心血管病医院 

单位级别:

三甲 

Institution
hospital:

Shanxi Cardiovascular Diseases Hospital

Level of the institution:

Teritary A

国家:

中国

省(直辖市):

山西 

市(区县):

 

Country:

China 

Province:

Shanxi 

City:

 

单位(医院):

山西医科大学第一医院 

单位级别:

三甲 

Institution
hospital:

First Hospital of Shanxi Medical University

Level of the institution:

Teritary A

国家:

中国

省(直辖市):

陕西 

市(区县):

 

Country:

China 

Province:

Shaanxi 

City:

 

单位(医院):

空军军医大学第二医院 

单位级别:

三甲 

Institution
hospital:

The Second Affiliated Hospital of Air Force Medical University

Level of the institution:

Teritary A

国家:

中国

省(直辖市):

北京 

市(区县):

 

Country:

China 

Province:

Beijing 

City:

 

单位(医院):

北京安贞医院 

单位级别:

三甲 

Institution
hospital:

Beijing Anzhen Hospital

Level of the institution:

Teritary A

国家:

中国

省(直辖市):

上海 

市(区县):

 

Country:

China 

Province:

Shanghai 

City:

 

单位(医院):

上海胸科医院 

单位级别:

三甲 

Institution
hospital:

Shanghai Chest Hospital

Level of the institution:

Teritary A

国家:

中国

省(直辖市):

河南 

市(区县):

 

Country:

China 

Province:

He'nan 

City:

 

单位(医院):

郑州大学第一附属医院 

单位级别:

三甲 

Institution
hospital:

The First Affiliated Hospital of Zhengzhou University

Level of the institution:

Teritary A

测量指标:

Outcomes:

指标中文名:

首次消融术后90天以后记录到首次临床复发的事件时间分析

指标类型:

主要指标

Outcome:

the first documented clinical recurrence occurring more than 90 days after the index ablation 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:

手术相关人员使用辐射防护设备的时间

指标类型:

次要指标

Outcome:

Time of radioprotective apron usage in procedure-related staff

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

消融后前90天内发生房颤/房扑/房速心律的患者比例

指标类型:

次要指标

Outcome:

proportion of patients with AF/AFL/ATa occurring during the first 90 days post ablation

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

因房颤/房扑/房速心律的复发,再次消融手术事件

指标类型:

次要指标

Outcome:

Repeat ablation procedure due to recurrence of AF/AFL/ATa

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

总手术时间

指标类型:

次要指标

Outcome:

Total procedure duration

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

X射线暴露时间

指标类型:

次要指标

Outcome:

X-ray exposure time

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

肺静脉隔离时间

指标类型:

次要指标

Outcome:

PV isolation time

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

围手术期并发症的发生率

指标类型:

次要指标

Outcome:

Incidence of peri-procedural complications

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

生活质量

指标类型:

次要指标

Outcome:

Quality of Life

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:

不适用

组织:

Sample Name:

NA

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:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 75 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):

中心随机

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

Central Randomization

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:

开放

Blinding:

Open

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

No

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):

试验完成后6个月内,通过ResMan提供原始数据查询, http://www.medresman.org

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

Six months after the trial complete,IPD will be public accessable 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:

原始记录表,电子采集和管理系统

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

Case Record Form, Electronic Data Capture

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2020-06-07 10:47:17