替罗非班治疗反复短暂性脑缺血发作的安全性及有效性研究

注册号:

Registration number:

ChiCTR-ONN-17013512 

最近更新日期:

Date of Last Refreshed on:

2017-11-23 21:49:32 

注册时间:

Date of Registration:

2017-11-23 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

替罗非班治疗反复短暂性脑缺血发作的安全性及有效性研究

Public title:

Safety and Efficacy of Intravenous Tirofiban in Patients with Recurrent Transient Ischemic Attack

注册题目简写:

ATTACK

English Acronym:

ATTACK

研究课题的正式科学名称:

替罗非班治疗反复短暂性脑缺血发作的安全性及有效性研究

Scientific title:

Safety and Efficacy of Intravenous Tirofiban in Patients with Recurrent Transient Ischemic Attack

研究课题代号(代码):

Study subject ID:

重庆市科委课题(CSTC2015shmszx120089)

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:

李玮 

研究负责人:

张猛 

Applicant:

Wei Li 

Study leader:

Meng Zhang 

申请注册联系人电话:

Applicant telephone:

+86 023 68767816

研究负责人电话:

Study leader's
telephone:

+86 023 68757816

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:

weili.tmmu@qq.com

研究负责人电子邮件:

Study leader's E-mail:

172228621@qq.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:

重庆市渝中区大坪长江支路10号

研究负责人通讯地址:

重庆市渝中区大坪长江支路10号

Applicant address:

10 Changjiang Branch Road, Yuzhong District, Chongqing, China

Study leader's address:

10 Changjiang Branch Road, Yuzhong District, Chongqing, 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:

第三军医大学大坪医院神经内科

Applicant's institution:

Neurology Department of Daping Hospital, Third Military Medical University

研究负责人所在单位:

第三军医大学大坪医院神经内科

Affiliation of the Leader:

Neurology Department of Daping Hospital, Third Military Medical 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:

2017-09

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:

第三军医大学大坪医院伦理委员会

Name of the ethic committee:

The Medical Ethics Committee of Daping Hospital, Third Military Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2017-01-12 00:00:00

伦理委员会联系人:

范士志

Contact Name of the ethic committee:

ShiZhi Fan

伦理委员会联系地址:

重庆市渝中区大坪长江支路10号

Contact Address of the ethic committee:

10 Changjiang Branch Road, Yuzhong District, Chongqing, 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:

第三军医大学大坪医院

Primary sponsor:

Da Ping Hospital of Third Military Medical University

研究实施负责(组长)单位地址:

重庆市渝中区大坪长江支路10号

Primary sponsor's address:

10 Changjiang Branch Road, Yuzhong District, Chongqing, 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):

重庆

市(区县):

Country:

China

Province:

Chongqing

City:

单位(医院):

第三军医大学大坪医院

具体地址:

重庆市渝中区大坪长江支路10号

Institution
hospital:

Daping hospital, Third Military Medical University

Address:

10 Changjiang Branch Road, Yuzhong District, Chongqing, China

国家:

中国

省(直辖市):

江苏

市(区县):

苏州

Country:

China

Province:

Jiangsu

City:

SuZhou

单位(医院):

苏州大学附属第二医院

具体地址:

江苏省苏州市三香路1055号

Institution
hospital:

The second affiliated hospital of Soochow University

Address:

1055 Sanxiang Road, Suzhou, Jiangsu, China

国家:

中国

省(直辖市):

吉林

市(区县):

长春

Country:

China

Province:

Jilin

City:

Changchun

单位(医院):

吉林大学中日联谊医院

具体地址:

吉林省长春市仙台大街126号

Institution
hospital:

China-Japan Union Hospital

Address:

126 Xiantai Street, Changchun

经费或物资来源:

重庆市科委课题(CSTC2015shmszx120089)

Source(s) of funding:

Chongqing Science & Technology Grant (CSTC2015shmszx120089)

研究疾病:

短暂性脑缺血发作  

Target disease:

Transient Ischemic Attack

研究疾病代码:

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

治疗新技术临床试验 

Study phase:

New Treatment Measure Clinical Study

研究设计:

非随机对照试验 

Study design:

Non randomized control 

研究目的:

观察替罗非班治疗反复短暂性脑缺血发作的安全性及有效性  

Objectives of Study:

To investigate the safety and efficacy of intravenous tirofiban in patients with recurrent transient ischemic attack

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:

1.起病时间4.5小时内,到院时最后一次症状持续超过1小时。
2.既往卒中遗留功能障碍,mRS≥2;
3.既往严重内脏出血及大手术30以内者;
4.合并严重疾病预期寿命小于一年者;
5.有遗传性出血倾向,口服抗凝药物且 INR > 1.7者;
6.血小板计数< 100,000/mm3;
7.血红蛋白 < 10 g/dL ;
8.血糖 ≤ 50 mg/dl ;
9.严重肾损害肌酐清除率<30ml/min;
10.家属或患者拒绝使用替罗非班者。

Exclusion criteria:

1) The last episode continued more than 1 hour but less than 4.5 hours when arrived the hospital;
2) Pre-stroke mRS ≥ 2;
3) History of severe bleeding or major surgery within 30 days;
4) Coexistent terminal illness with life expectancy ≤ 12 months;
5) Any known hereditary or acquired hemorrhagic diathesis, coagulation factor deficiency, or taking oral anticoagulant with INR > 1.7;
6) Platelet count < 100,000/mm3;
7) Hemoglobin < 10 g/dL;
8) A serum glucose level≤ 50 mg/dl; or
9) Severe renal insufficiency with creatinine clearance rate <30ml/min;
10) Patient or his/her relative refused to use tirofiban.

研究实施时间:

Study execute time:

From 2017-12-01 00:00:00 To 2019-05-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2017-12-01 00:00:00 To 2019-08-31 00:00:00

干预措施:

Interventions:

组别:

替罗非班组

样本量:

40

Group:

tirofiban group

Sample size:

干预措施:

静脉替罗非班

干预措施代码:

Intervention:

intravenous tirofiban

Intervention code:

组别:

对照

样本量:

40

Group:

Control

Sample size:

干预措施:

单纯扩容、口服抗血小板或抗凝治疗

干预措施代码:

Intervention:

expansion only, oral antiplatelet or anticoagulant therapy

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

重庆 

市(区县):

 

Country:

China

Province:

Chongqing

City:

单位(医院):

第三军医大学大坪医院 

单位级别:

三甲 

Institution
hospital:

Daping hospital,Third Military Medical University

Level of the institution:

Tertiary A hospital

国家:

中国

省(直辖市):

江苏 

市(区县):

苏州 

Country:

China

Province:

Jiangsu

City:

Suzhou

单位(医院):

苏州大学第二附属医院 

单位级别:

三甲 

Institution
hospital:

The second affiliated hospital of Soochow University

Level of the institution:

Tertiary A hospital

国家:

中国

省(直辖市):

吉林 

市(区县):

长春 

Country:

China

Province:

Jilin

City:

Changchun

单位(医院):

吉林大学中日联谊医院 

单位级别:

三甲 

Institution
hospital:

China-Japan Union Hospital

Level of the institution:

Tertiary A hospital

测量指标:

Outcomes:

指标中文名:

颅内出血转化

指标类型:

主要指标

Outcome:

intracerebral hemorrhage transformation

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

NIHSS评分

指标类型:

主要指标

Outcome:

NIHSS score

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

mRS

指标类型:

主要指标

Outcome:

mRS

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

缺血事件发作次数

指标类型:

主要指标

Outcome:

times of the reccurrent ischemic events

Type:

Primary 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:

组织:

Sample Name:

none

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 18 years
最大 Max age 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):

非随机对照

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

non randomized contral

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):

2019年2月28日,上传原始数据excel表格

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

02-28-2019 unload excel

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:

仅CRF

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

only CRF

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2017-11-23 21:49:23