评价保护性肺通气策略对全麻术后认知障碍的影响

注册号:

Registration number:

ChiCTR1900021155 

最近更新日期:

Date of Last Refreshed on:

2019-01-30 20:59:47 

注册时间:

Date of Registration:

2019-01-30 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

评价保护性肺通气策略对全麻术后认知障碍的影响

Public title:

To evaluate the effect of protective pulmonary ventilation strategy on cognitive impairment after general anesthesia

注册题目简写:

English Acronym:

研究课题的正式科学名称:

评价保护性肺通气策略对全麻术后认知障碍的影响

Scientific title:

To evaluate the effect of protective pulmonary ventilation strategy on cognitive impairment after general anesthesia

研究课题代号(代码):

Study subject ID:

河北省政府资助临床优秀人才培养和基础课题研究项目(361005)

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:

王静 

研究负责人:

王秋筠 

Applicant:

Jing Wang 

Study leader:

Qiujun Wang 

申请注册联系人电话:

Applicant telephone:

+86 18330101163

研究负责人电话:

Study leader's
telephone:

+86 18533112929

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:

402934866@qq.com

研究负责人电子邮件:

Study leader's E-mail:

13933178001@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:

河北省石家庄市桥西区自强路139号

研究负责人通讯地址:

河北省石家庄市桥西区自强路139号

Applicant address:

139 Ziqiang Road, Qiaoxi District, Shijiazhuang, Hebei, China

Study leader's address:

139 Ziqiang Road, Qiaoxi District, Shijiazhuang, Hebei, China

申请注册联系人邮政编码:

Applicant postcode:

050051

研究负责人邮政编码:

Study leader's postcode:

050051

申请人所在单位:

河北医科大学第三医院

Applicant's institution:

The Third Hospital of Hebei Medical University

研究负责人所在单位:

河北医科大学第三医院

Affiliation of the Leader:

The Third Hospital of Hebei 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:

2018-033-1

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:

河北医科大学第三医院伦理委员会

Name of the ethic committee:

Ethic Committee of the Third Hospital of Hebei Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2018-12-27 00:00:00

伦理委员会联系人:

郑金

Contact Name of the ethic committee:

Jin Zheng

伦理委员会联系地址:

河北省石家庄市桥西区自强路139号

Contact Address of the ethic committee:

139 Ziqiang Road, Shijiazhuang, Hebei, 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:

河北医科大学第三医院

Primary sponsor:

The Third Hospital of Hebei Medical University

研究实施负责(组长)单位地址:

河北省石家庄市桥西区自强路139号

Primary sponsor's address:

139 Ziqiang Road, Qiaoxi District, Shijiazhuang, Hebei, 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):

河北省

市(区县):

石家庄市

Country:

China

Province:

Hebei

City:

Shijiazhuang city

单位(医院):

河北医科大学第三医院

具体地址:

河北省石家庄市桥西区自强路139号

Institution
hospital:

The Third Hospital of Hebei Medical University

Address:

139 Ziqiang Road, Qiaoxi District, Shijiazhuang, Hebei, China

经费或物资来源:

河北省政府资助临床优秀人才培养和基础课题研究项目(361005)

Source(s) of funding:

Hebei Provincial Government Funded Clinical Talents Cultivation and Basic Research Projects(361005)

研究疾病:

术后认知障碍  

Target disease:

Postperative cognitive impairment

研究疾病代码:

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:

随机平行对照 

Study design:

Parallel 

研究目的:

本研究拟评价保护性肺通气策略对全麻患者术后认知障碍的影响。  

Objectives of Study:

The aim of this study is to evaluate the effect of protective pulmonary ventilation strategy on cognitive impairment after general anesthesia.

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)有慢性疼痛史、中枢神经和心理疾病史、应用抗抑郁药和镇静药物史、帕金森病史、癫痫病史,术前有低氧血症、慢性肺部疾病及哮喘病史(2)手术时间超过4小时(3)术中出血量超过800mL(4)手术因各种原因被取消

Exclusion criteria:

1. A history of chronic pain, central nervous and mental illness, use of antidepressants and sedatives, Parkinson's disease, epilepsy, and preoperative hypoxemia, chronic pulmonary disease, and asthma;
2. The operation time more than four hours;
3. Intraoperative blood loss exceed 800mL;
4. The operation is cancelled for various reasons.

研究实施时间:

Study execute time:

From 2019-03-01 00:00:00 To 2021-06-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2019-03-01 00:00:00 To 2021-06-30 00:00:00

干预措施:

Interventions:

组别:

对照组

样本量:

40

Group:

Group 1

Sample size:

干预措施:

标准治疗

干预措施代码:

Intervention:

Standdard treatment

Intervention code:

组别:

保护性肺通气组

样本量:

40

Group:

Group 2

Sample size:

干预措施:

保护性肺通气

干预措施代码:

Intervention:

Protective pulmonary ventilation

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

河北省 

市(区县):

石家庄市 

Country:

China

Province:

Hebei

City:

Shijiazhuang

单位(医院):

河北医科大学第三医院 

单位级别:

三级甲等 

Institution
hospital:

The Third Hospital of Hebei Medical University

Level of the institution:

Tertiary A hospital

测量指标:

Outcomes:

指标中文名:

氧分压

指标类型:

主要指标

Outcome:

Oxygen partial pressure

Type:

Primary indicator

测量时间点:

测量方法:

动脉血气

Measure time point of outcome:

Measure method:

指标中文名:

二氧化碳分压

指标类型:

主要指标

Outcome:

PCO2

Type:

Primary indicator

测量时间点:

测量方法:

动脉血气

Measure time point of outcome:

Measure method:

指标中文名:

血氧饱和度

指标类型:

主要指标

Outcome:

Oxygen saturation

Type:

Primary indicator

测量时间点:

测量方法:

动脉血气

Measure time point of outcome:

Measure method:

指标中文名:

乳酸

指标类型:

主要指标

Outcome:

Lactic acid

Type:

Primary indicator

测量时间点:

测量方法:

动脉血气

Measure time point of outcome:

Measure method:

指标中文名:

白细胞介素6

指标类型:

主要指标

Outcome:

IL-6

Type:

Primary indicator

测量时间点:

测量方法:

酶联免疫法

Measure time point of outcome:

Measure method:

指标中文名:

白细胞介素8

指标类型:

主要指标

Outcome:

IL-8

Type:

Primary indicator

测量时间点:

测量方法:

酶联免疫法

Measure time point of outcome:

Measure method:

指标中文名:

肺泡表面活性物质A

指标类型:

主要指标

Outcome:

SP-A

Type:

Primary indicator

测量时间点:

测量方法:

酶联免疫法

Measure time point of outcome:

Measure method:

指标中文名:

认知功能

指标类型:

主要指标

Outcome:

Cognitive function

Type:

Primary indicator

测量时间点:

测量方法:

MMSE评分

Measure time point of outcome:

Measure method:

指标中文名:

胶质纤维酸性蛋白

指标类型:

主要指标

Outcome:

GFAP

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

克拉拉细胞蛋白

指标类型:

主要指标

Outcome:

CC16

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:

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:

尚未开始

Not yet 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):

由专业技术人员采用随机数字表法对纳入患者进行分组

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

The included patients will be divided into groups by professional technicians using random number table method

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:

未说明

Blinding:

Not stated

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):

实验结束后6个月内使用ResMan进行原始数据共享

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

ResMan will be used for raw data sharing within 6 months after the end of the experiment

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:

实验结束后6个月使用ResMan进行原始数据管理

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

ResMan will be used for raw data management six months after the end of the experiment

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2019-01-30 20:59:47