ChiCTR2400091313 版本V1.0 版本创建时间2024/10/25 11:41:37 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:

ChiCTR2400091313 

最近更新日期:

Date of Last Refreshed on:

2024-10-25 11:41:19 

注册时间:

Date of Registration:

2024-10-25 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

甲苯磺酸瑞马唑仑对老年腹部大手术术后认知功能的影响

Public title:

Effect of remimazolam tosylate on cognitive function after major abdominal surgery in older adults

注册题目简写:

瑞马唑仑对术后认知功能的影响

English Acronym:

Effect of remimazolam on postoperative cognitive function

研究课题的正式科学名称:

甲苯磺酸瑞马唑仑对老年腹部大手术术后认知功能的影响

Scientific title:

Effect of remimazolam tosylate on cognitive function after major abdominal surgery in older adults

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:

张克尧 

研究负责人:

张克尧 

Applicant:

Keyao Zhang 

Study leader:

Keyao Zhang 

申请注册联系人电话:

Applicant telephone:

+86 195 5215 3301

研究负责人电话:

Study leader's telephone:

+86 195 5215 3301

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:

695055042@qq.com

研究负责人电子邮件:

Study leader's E-mail:

695055042@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:

连云港市海州区振华东路6号

研究负责人通讯地址:

连云港市海州区振华东路6号

Applicant address:

No. 6, Zhenhua East Road, Haizhou District, Lianyungang City

Study leader's address:

No. 6, Zhenhua East Road, Haizhou District, Lianyungang City

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:

连云港市第一人民医院

Applicant's institution:

The First People's Hospital of Lianyungang

研究负责人所在单位:

连云港市第一人民医院

Affiliation of the Leader:

The First People's Hospital of Lianyungang

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:

KY-20240801001-02

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:

连云港市第一人民医院医学伦理委员会

Name of the ethic committee:

Medical Ethics Committee of the First People's Hospital of Lianyungang City

伦理委员会批准日期:

Date of approved by ethic committee:

2024-09-12 00:00:00

伦理委员会联系人:

高山

Contact Name of the ethic committee:

Shan Gao

伦理委员会联系地址:

连云港市振华东路 6 号连云港市第一人民医院高新 区院区 4 号楼 2 楼

Contact Address of the ethic committee:

2nd Floor, Building 4, High-tech District Campus, Lianyungang First People's Hospital, No. 6 Zhenhua East Road, Lianyungang City

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 189 6132 2336

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:

连云港市第一人民医院

Primary sponsor:

The First People's Hospital of Lianyungang

研究实施负责(组长)单位地址:

连云港市海州区振华东路6号

Primary sponsor's address:

No. 6, Zhenhua East Road, Haizhou District, Lianyungang City

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

江苏省

市(区县):

Country:

China

Province:

Jiangsu

City:

单位(医院):

连云港市第一人民医院

具体地址:

江苏省连云港市海州区振华东路6号

Institution
hospital:

The First People's Hospital of Lianyungang

Address:

No. 6, Zhenhua East Road, Haizhou District, Lianyungang City

经费或物资来源:

自筹

Source(s) of funding:

Self-funded

Target disease:

Postoperative cognitive dysfunction

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

上市后药物 

Study phase:

4

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

探讨瑞马唑仑对老年腹部大手术术后认知功能的影响,为降低该群体术后神经认知功能损害提供临床依据  

Objectives of Study:

To investigate the effect of remimazolam on the cognitive function of elderly people after major abdominal surgery, so as to provide a clinical basis for reducing the postoperative neurocognitive impairment in this group

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≥65岁和<90岁; ②手术前未进行任何放疗或化疗的原发癌; ③采用全身麻醉,且手术预计时间>2h者。

Inclusion criteria

(1) Age≥ 65 years old and < 90 years old; (2) Primary cancer that has not undergone any radiotherapy or chemotherapy before surgery; (3) Those who use general anesthesia and the estimated time of surgery > 2 hours.

排除标准:

①术前有精神分裂症、癫痫、帕金森氏症、重症肌无力或诊断明确的抑郁症病史; ②因昏迷、严重痴呆、语言障碍、精神错乱或严重疾病导致无法正常沟通; ③危重疾病(术前ASA身体状况分级>3级)、严重肝功能障碍(Child-C级)或严重肾功能障碍(术前进行透析); ④具有神经外科手术史; ⑤精神类药品滥用史。

Exclusion criteria:

(1) Have a history of schizophrenia, epilepsy, Parkinson's disease, myasthenia gravis, or well-diagnosed depression before surgery; (2) Inability to communicate normally due to coma, severe dementia, speech disorder, mental disorder or serious illness; (3) Critical illness (preoperative ASA physical condition classification > grade 3), severe liver dysfunction (Child-C grade) or severe renal dysfunction (preoperative dialysis); (4) Have a history of neurosurgery; (5) History of psychotropic drug abuse.

研究实施时间:

Study execute time:

From 2024-07-01 00:00:00 To 2026-07-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2024-10-30 00:00:00 To 2026-05-31 00:00:00  

干预措施:

Interventions:

组别:

瑞马唑仑组

样本量:

267

Group:

Remimazolam group

Sample size:

干预措施:

瑞马唑仑组(R组),麻醉诱导、维持采用瑞马唑仑。额外用药包含舒芬太尼、依托咪酯、维库溴铵。

干预措施代码:

Intervention:

Remimazolam group (R group), anesthesia induction and maintenance were treated with remimazolam. Additional medications include sufentanil, etomidate, and vecuronium.

Intervention code:

组别:

丙泊酚组

样本量:

267

Group:

Propofol group

Sample size:

干预措施:

丙泊酚组(P组),麻醉诱导、维持采用丙泊酚。额外用药包含舒芬太尼、依托咪酯、维库溴铵。

干预措施代码:

Intervention:

Propofol group (P group), anesthesia induction and maintenance were treated with propofol. Additional medications include sufentanil, etomidate, and vecuronium.

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

江苏 

市(区县):

 

Country:

China 

Province:

Jiangsu 

City:

 

单位(医院):

连云港市第一人民医院 

单位级别:

三甲 

Institution
hospital:

The First People's Hospital of Lianyungang

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

术后认知障碍的发生率

指标类型:

主要指标

Outcome:

The incidence of postoperative cognitive dysfunction

Type:

Primary indicator

测量时间点:

术后 1 周

测量方法:

Measure time point of outcome:

1 week after surgery

Measure method:

指标中文名:

术后谵妄发生率

指标类型:

次要指标

Outcome:

Postoperative delirium incidence rate

Type:

Secondary indicator

测量时间点:

3 天内

测量方法:

Measure time point of outcome:

Within 3 days

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

其它  

说明

Fate of sample:

0thers  

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 90 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):

一位独立于数据管理和统计分析的研究员通过使用来自www.randomization.com的工具,生成随机数(1:1比例,区块大小为4)以对患者进行分组。

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

A researcher independent of data management and statistical analysis generates random numbers (1:1 scale with a block size of 4) to group patients by using a tool from www.randomization.com.

是否公开试验完成后的统计结果:

Calculated Results after the Study Completed public access:

不公开/Private

盲法:

单盲,

Blinding:

Single-blind

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):

ResMan, http://www.medresman.org.cn/login.aspx

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

ResMan, http://www.medresman.org.cn/login.aspx

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:

问卷调查

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

Questionnaire

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2024-10-25 11:41:19