ChiCTR2000032838 版本V1.0 版本创建时间2020/05/12 15:19:11 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:

ChiCTR2000032838 

最近更新日期:

Date of Last Refreshed on:

2020-05-12 15:19:05 

注册时间:

Date of Registration:

1990-01-01 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

急性期他汀使用与卒中后肺炎的联系

Public title:

Association between statin treatment in the acute phase and poststroke pneumonia

注册题目简写:

English Acronym:

研究课题的正式科学名称:

急性期他汀使用与卒中后肺炎的联系

Scientific title:

Association between statin treatment in the acute phase and poststroke pneumonia

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:

李昌玲 

研究负责人:

李昌玲 

Applicant:

Changling Li 

Study leader:

Changling Li 

申请注册联系人电话:

Applicant telephone:

18328084863

研究负责人电话:

Study leader's telephone:

18328084863

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:

1764974717@qq.com

研究负责人电子邮件:

Study leader's E-mail:

1764974717@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:

四川省成都市武侯区国学巷37号

研究负责人通讯地址:

四川省成都市武侯区国学巷37号

Applicant address:

No.37 Guoxue Lane, Wuhou District, Chengdu City, Sichuan Province

Study leader's address:

No.37 Guoxue Lane, Wuhou District, Chengdu City, Sichuan Province

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:

四川大学华西医院

Applicant's institution:

West China Hospital of Sichuan University

研究负责人所在单位:

Affiliation of the Leader:

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:

2019年审(319)号

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:

四川大学华西医院生物医学伦理审查委员会

Name of the ethic committee:

Ethics Committee on Biomedical Research, West China Hospital of Sichuan 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:

杜陵江

Contact Name of the ethic committee:

Lingjiang Du

伦理委员会联系地址:

四川省成都市人民南路三段17号

Contact Address of the ethic committee:

No.17, Section 3, Renmin South Road, Chengdu City, Sichuan Province

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:

四川大学华西医院

Primary sponsor:

West China Hospital of Sichuan University

研究实施负责(组长)单位地址:

四川省成都市武侯区国学巷37号

Primary sponsor's address:

No.37 Guoxue Lane, Wuhou District, Chengdu City, Sichuan Province

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

四川

市(区县):

成都

Country:

China

Province:

Sichuan

City:

Chengdu

单位(医院):

四川大学华西医院

具体地址:

武侯区国学巷37号

Institution
hospital:

West China Hospital of Sichuan University

Address:

37 Guoxue Lane, Wuhou District

经费或物资来源:

Source(s) of funding:

No

Target disease:

poststroke pneumonia

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

回顾性研究 

Study phase:

Retrospective study

研究设计:

队列研究 

Study design:

Cohort study 

研究目的:

探讨急性期他汀使用对卒中后肺炎的发生风险、严重程度、临床结局的影响。  

Objectives of Study:

To investigate the effect of statin in the acute phase on the risk, severity and clinical outcome of poststroke pneumonia.

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.确诊首次急性缺血性卒中并于3天内住院;2.年龄≥18岁;

Inclusion criteria

(1) acute ischemic stroke diagnosed on admission according to the World Health Organization (WHO) criteria; (2) age ≥ 18 years; and (3) time from onset to admission ≤ 3 days.

排除标准:

1.年龄<18岁;2.卒中前或住院期间预防性使用了抗生素;3.患有感染性疾病或免疫性疾病;4.接受了免疫球蛋白治疗或免疫抑制药物;5.非急性期内使用了他汀;6.卒中后肺炎外的卒中后的感染;7.妊娠。

Exclusion criteria:

(1) a history of stroke or transient ischemic attack (TIA); (2) prophylactic antibiotics therapy before stroke or during hospitalization; (3) suffering from infectious or immunologic disease before stroke, or receiving immunoglobulin therapies or immunosuppressive medications; (4) statin treatment during non-acute phase (prior to stroke onset or at a later time point during the hospital stays); (5) pregnancy; and (6) other post-stroke infections (non-SAP).

研究实施时间:

Study execute time:

From 2020-03-01 00:00:00 To 2020-06-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2020-05-01 00:00:00 To 2020-06-30 00:00:00  

干预措施:

Interventions:

组别:

卒中后肺炎组VS无卒中后肺炎组

样本量:

1200

Group:

poststroke pneumonia group vs. non poststroke pneumonia group

Sample size:

干预措施:

干预措施代码:

Intervention:

Nil

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

四川 

市(区县):

成都 

Country:

China 

Province:

Sichuan 

City:

Chengdu 

单位(医院):

四川大学华西医院 

单位级别:

三甲 

Institution
hospital:

West China Hospital of Sichuan University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

卒中后肺炎的发生风险

指标类型:

主要指标

Outcome:

the risk of poststroke pneumonia

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

卒中后肺炎的90天临床结局

指标类型:

主要指标

Outcome:

clinicaloutcome of poststroke pneumonia at 90 days

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

卒中后肺炎的严重程度

指标类型:

次要指标

Outcome:

poststroke pneumonia severity

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:

组织:

Sample Name:

N/A

Tissue:

人体标本去向

其它  

说明

Fate of sample:

0thers  

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 96 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):

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

No

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

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):

预计2020年底公开原始数据,可供合理索取

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

Raw data is expected to be made available for reasonable access by the end of 2020

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:

病例记录表

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

Case Record Form, CRF

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:

 2020-05-12 15:19:05