ChiCTR1900022742 版本V1.1 版本创建时间2019/04/24 13:48:01 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:

ChiCTR1900022742 

最近更新日期:

Date of Last Refreshed on:

2019-04-24 13:45:08 

注册时间:

Date of Registration:

2019-04-24 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

心脏手术术后导管相关性感染危险因素研究

Public title:

Study for the risk factors of device-associated health care-associated infections after cardiac surgery

注册题目简写:

English Acronym:

研究课题的正式科学名称:

心脏手术术后导管相关性感染危险因素研究

Scientific title:

Study for the risk factors of device-associated health care-associated infections after cardiac surgery

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:

袁素 

研究负责人:

袁素 

Applicant:

Su Yuan 

Study leader:

Su Yuan 

申请注册联系人电话:

Applicant telephone:

+86 13621019302

研究负责人电话:

Study leader's telephone:

+86 13621019302

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:

13621019302@163.com

研究负责人电子邮件:

Study leader's E-mail:

13621019302@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:

北京市西城区北礼士路167号

研究负责人通讯地址:

北京市西城区北礼士路167号

Applicant address:

167 Lishi Road North, Xicheng District, Beijing, China

Study leader's address:

167 Lishi Road North, Xicheng District, Beijing, China

申请注册联系人邮政编码:

Applicant postcode:

100037

研究负责人邮政编码:

Study leader's postcode:

100037

申请人所在单位:

中国医学科学院阜外医院

Applicant's institution:

Fuwai Hospital, Chinese Academy of Medical Sciences

研究负责人所在单位:

中国医学科学院阜外医院

Affiliation of the Leader:

Fuwai Hospital, Chinese Academy of Medical Sciences

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:

2018-1073

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:

中国医学科学院阜外医院伦理委员会

Name of the ethic committee:

Ethics Committee of Fuwai Hospital, Chinese Academy of Medical Sciences

伦理委员会批准日期:

Date of approved by ethic committee:

2019-01-23 00:00:00

伦理委员会联系人:

赵志晶

Contact Name of the ethic committee:

Zhijing Zhao

伦理委员会联系地址:

北京市西城区北礼士路167号

Contact Address of the ethic committee:

167 Lishi Road North, Xicheng District, Beijing, 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:

中国医学科学院阜外医院

Primary sponsor:

Fuwai Hospital, Chinese Academy of Medical Sciences

研究实施负责(组长)单位地址:

北京市西城区北礼士路167号

Primary sponsor's address:

167 Lishi Road North, Xicheng District, Beijing, 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):

北京

市(区县):

西城区

Country:

China

Province:

Beijing

City:

Xicheng District

单位(医院):

中国医学科学院阜外医院

具体地址:

北礼士路167号

Institution
hospital:

Fuwai Hospital, Chinese Academy of Medical Sciences

Address:

167 Lishi Road North, Xicheng District

经费或物资来源:

深圳市益心达医学新技术有限公司

Source(s) of funding:

SCW Medicath Ltd

Target disease:

device-associated health care-associated infections after cardiac surgery

Target disease code:

研究类型:

基础科学研究

Study type:

Basic Science

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

连续入组 

Study design:

Sequential 

研究目的:

(1)明确DA-HAIs在本中心成人心脏ICU的发生率; (2)探索DA-HAIs对ICU停留时间、医疗花费及短期预后的影响; (3)分析DA-HAIs发生相关的围术期预测因素。  

Objectives of Study:

(1)To determine the incidence of DA-HAIs in the adult cardiac ICU of the center (2)To explore the effect of DA-HAIs on duration of ICU stay, medical cost and short-term prognosis (3)To analyze the perioperative predictors of the occurrence of DA-HAIs

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)拟行心血管手术;
(2)拟进入成人心脏外科ICU。

Inclusion criteria

(1)Planning to undergo cardiac surgery;
(2)Planning to enter the adult cardiac surgery ICU.

排除标准:

Exclusion criteria:

no

研究实施时间:

Study execute time:

From 2019-05-01 00:00:00 To 2021-01-22 00:00:00  

征募观察对象时间:

Recruiting time:

From 2019-05-01 00:00:00 To 2021-01-22 00:00:00  

干预措施:

Interventions:

组别:

Case series

样本量:

100

Group:

Case series

Sample size:

干预措施:

干预措施代码:

Intervention:

No

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

北京 

市(区县):

西城区 

Country:

China 

Province:

Beijing 

City:

Xicheng district 

单位(医院):

中国医学科学院阜外医院 

单位级别:

三甲医院 

Institution
hospital:

Fuwai Hospital, Chinese Academy of Medical Sciences

Level of the institution:

Tertiary A Hospital

测量指标:

Outcomes:

指标中文名:

中心静脉导管相关性感染

指标类型:

主要指标

Outcome:

central lineeassociated bloodstream infection

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

呼吸机相关肺炎

指标类型:

主要指标

Outcome:

ventilator-associated 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:

导管相关尿路感染

指标类型:

主要指标

Outcome:

catheter-associated urinary tract infection

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

住院时间

指标类型:

次要指标

Outcome:

length of stay

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

住院花费

指标类型:

次要指标

Outcome:

hospitalization costs

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

ICU停留时间

指标类型:

次要指标

Outcome:

ICU length of stay

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术后并发症

指标类型:

次要指标

Outcome:

postoperative 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:

术后死亡率

指标类型:

次要指标

Outcome:

the incidence of hospitalization mortality

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:

标本中文名:

尿液

组织:

Sample Name:

Urine

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 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):

序贯性连续入组

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

sequential

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:

N/A

Blinding:

N/A

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):

2021年7月,中国临床试验注册中心

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

Jul. 2021, Chinese clinical trial registry

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:

病例记录表采集数据,access软件管理数据

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

Case Record Form collects data, access software manages data

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2019-04-24 13:44:39