醒脑静注射液治疗大面积脑梗死有效性及安全性的回顾性研究

注册号:

Registration number:

ChiCTR2400092367 

最近更新日期:

Date of Last Refreshed on:

2024-11-14 16:38:48 

注册时间:

Date of Registration:

2024-11-14 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

醒脑静注射液治疗大面积脑梗死有效性及安全性的回顾性研究

Public title:

A retrospective Study on the Efficacy and Safety of Xingnaojing Injection in the Treatment of large hemispheric infarction

注册题目简写:

English Acronym:

研究课题的正式科学名称:

醒脑静注射液治疗大面积脑梗死有效性及安全性的回顾性研究

Scientific title:

A retrospective Study on the Efficacy and Safety of Xingnaojing Injection in the Treatment of large hemispheric infarction

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:

李晶 

研究负责人:

李晶 

Applicant:

Jing Li 

Study leader:

Jing Li 

申请注册联系人电话:

Applicant telephone:

+86 157 2706 7053

研究负责人电话:

Study leader's
telephone:

+86 157 2706 7053

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:

synapses1991@126.com

研究负责人电子邮件:

Study leader's E-mail:

synapses1991@126.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:

湖北省武汉市洪山区珞喻路856号湖北省中医院新住院大楼五楼重症医学科医生办

研究负责人通讯地址:

湖北省武汉市洪山区珞喻路856号湖北省中医院新住院大楼五楼重症医学科医生办

Applicant address:

ICU, Hubei Provincial Hospital of TCM, No. 856 Luoyu Road, Hongshan District, Wuhan, Hubei Province

Study leader's address:

ICU, Hubei Provincial Hospital of TCM, No. 856 Luoyu Road, Hongshan District, Wuhan, Hubei Province

申请注册联系人邮政编码:

Applicant postcode:

430000

研究负责人邮政编码:

Study leader's postcode:

430000

申请人所在单位:

湖北省中医院

Applicant's institution:

Hubei Provincial Hospital of TCM

研究负责人所在单位:

湖北省中医院

Affiliation of the Leader:

Hubei Provincial Hospital of TCM

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:

HBZY2024-C11-01

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:

湖北省中医院伦理委员会

Name of the ethic committee:

Ethics Committee of Hubei Provincial Hospital of TCM

伦理委员会批准日期:

Date of approved by ethic committee:

2024-03-05 00:00:00

伦理委员会联系人:

张馨

Contact Name of the ethic committee:

Xin Zhang

伦理委员会联系地址:

湖北省武汉市武昌区花园山4号湖北省中医院伦理委员会办公室

Contact Address of the ethic committee:

Office of the Ethics Committee of Hubei Provincial Hospital of TCM, No. 4 Huayuan Mountain, Wuchang District, Wuhan, Hubei Province

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 27 8892 0956

伦理委员会联系人邮箱:

Contact email of the ethic committee:

hbszyykyc@163.com

研究实施负责(组长)单位:

湖北省中医院

Primary sponsor:

Hubei Provincial Hospital of TCM

研究实施负责(组长)单位地址:

湖北省武汉市洪山区珞喻路856号湖北省中医院

Primary sponsor's address:

Hubei Provincial Hospital of TCM, No. 856 Luoyu Road, Hongshan District, Wuhan, Hubei 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):

湖北省

市(区县):

武汉市

Country:

China

Province:

Hubei

City:

Wuhan

单位(医院):

湖北省中医院

具体地址:

湖北省武汉市洪山区珞喻路856号湖北省中医院

Institution
hospital:

Hubei Provincial Hospital of TCM

Address:

Hubei Provincial Hospital of TCM, No. 856 Luoyu Road, Hongshan District, Wuhan, Hubei Province

经费或物资来源:

自筹

Source(s) of funding:

self-financing

研究疾病:

大面积脑梗死  

Target disease:

large hemispheric infarction

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:

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:

本项目为验证醒脑静注射液对大面积脑梗死患者的临床疗效,通过采用回顾性队列研究,为中医药防治大面积脑梗死的提供依据。  

Objectives of Study:

This project aims to verify the clinical efficacy of Xingnaojing in patients with LHI. Through a retrospective cohort study, it provides evidence-based evidence for the use of TCM in the prevention and treatment of LHI.

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:

由于肿瘤、外伤或蛛网膜下腔出血并发血管痉挛等病因所致大面积脑梗死的患者

Exclusion criteria:

Patients with extensive cerebral infarction caused by factors such as tumors, trauma, or subarachnoid hemorrhage complicated by vascular spasm

研究实施时间:

Study execute time:

From 2024-03-05 00:00:00 To 2025-03-05 00:00:00  

征募观察对象时间:

Recruiting time:

From 2024-11-20 00:00:00 To 2025-01-31 00:00:00

干预措施:

Interventions:

组别:

常规治疗组

样本量:

39

Group:

Conventional treatment group

Sample size:

干预措施:

干预措施代码:

Intervention:

NA

Intervention code:

组别:

醒脑静组

样本量:

40

Group:

Xingnaojing group

Sample size:

干预措施:

干预措施代码:

Intervention:

NA

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

湖北省 

市(区县):

武汉市 

Country:

China

Province:

Hubei

City:

Wuhan

单位(医院):

湖北省中医院 

单位级别:

三甲 

Institution
hospital:

Hubei Provincial Hospital of TCM

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

住院期间死亡率

指标类型:

主要指标

Outcome:

Mortality rate during hospitalization

Type:

Primary indicator

测量时间点:

出院时

测量方法:

出院时患者生存情况

Measure time point of outcome:

At discharge

Measure method:

Patient survival status at discharge

指标中文名:

出院mRS评分

指标类型:

主要指标

Outcome:

Discharge mRS score

Type:

Primary indicator

测量时间点:

出院时

测量方法:

使用mRS量表按照出院小结中患者症状体征进行评分

Measure time point of outcome:

At discharge

Measure method:

Use the mRS scale to score patients based on their symptoms and signs in the discharge summary

指标中文名:

住院天数

指标类型:

次要指标

Outcome:

Hospitalization days

Type:

Secondary indicator

测量时间点:

出院时

测量方法:

从入院至出院患者总体住院时长

Measure time point of outcome:

At discharge

Measure method:

Overall length of hospital stay for patients from admission to discharge

指标中文名:

中风证候积分疗效评定

指标类型:

次要指标

Outcome:

Evaluation of therapeutic effect of stroke syndrome integral

Type:

Secondary indicator

测量时间点:

醒脑静治疗前和醒脑静治疗结束后各评分一次

测量方法:

疗效=(治疗前评分—治疗后评分)/治疗前评分×100%,分基本恢复、显著进步、进步、稍进步、无变化、恶化

Measure time point of outcome:

Score once before and once after Xingnaojing treatment

Measure method:

Efficacy=(pre treatment score - post treatment score)/pre treatment score x 100%, with scores of basic recovery, significant progress, progress, slight progress, no change, deterioration

指标中文名:

血常规

指标类型:

副作用指标

Outcome:

Blood routine

Type:

Adverse events

测量时间点:

醒脑静治疗前和醒脑静治疗结束后各检查一次

测量方法:

记录醒脑静治疗前和醒脑静治疗结束后本院检验科血常规、肝肾功能、凝血功能检验结果

Measure time point of outcome:

Check once before and once after Xingnaojing treatment

Measure method:

Record the blood routine, liver and kidney function, and coagulation function test results of our hospital's laboratory before and after Xingnaojing treatment

指标中文名:

肝功能

指标类型:

副作用指标

Outcome:

liver function

Type:

Adverse events

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

肾功能

指标类型:

副作用指标

Outcome:

kidney function

Type:

Adverse events

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

凝血功能

指标类型:

副作用指标

Outcome:

coagulation function

Type:

Adverse events

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

其它  

说明

本研究为回顾性研究,不重新采集人体标本,血液检查指标(血常规、肝肾功能、凝血功能等)为住院期间检查结果

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 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):

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

None

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:

None

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

否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):

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

No

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:

采用病历记录表进行数据采集和管理

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

Using medical record forms for data collection and management

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2024-11-14 16:38:31