消栓肠溶胶囊治疗缺血性脑卒中的临床研究

注册号:

Registration number:

ITMCTR2024000096

最近更新日期:

Date of Last Refreshed on:

2024-06-06

注册时间:

Date of Registration:

2024-06-06

注册号状态:

Registration Status:

补注册

Retrospective registration

注册题目:

消栓肠溶胶囊治疗缺血性脑卒中的临床研究

Public title:

Clinical study of Xiaoshuan enteric-soluble capsule in the treatment of ischemic stroke

注册题目简写:

English Acronym:

研究课题的正式科学名称:

脑缺血缺氧性损害的机制与中医药防治研究

Scientific title:

Study on the mechanism of hypoxic injury caused by cerebral ischemia and its prevention and treatment with traditional Chinese medicine

研究课题的正式科学名称简写:

Scientific title acronym:

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:

温春丽

研究负责人:

胡风云

Applicant:

Chunli Wen

Study leader:

Fengyun Hu

申请注册联系人电话:

Applicant telephone:

13453421563

研究负责人电话:

Study leader's telephone:

13834233638

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:

871540776@qq.com

研究负责人电子邮件:

Study leader's E-mail:

fengyun71@163.com

申请单位网址(自愿提供):

Study leader's 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:

山西省太原市迎泽区双塔寺街29号

研究负责人通讯地址:

山西省太原市迎泽区双塔寺街29号

Applicant address:

29 Shuangtasi Street, Yingze Distrcit, Taiyuan,Shanxi

Study leader's address:

29 Shuangtasi Street, Yingze Distrcit, Taiyuan,Shanxi

申请注册联系人邮政编码:

Applicant postcode:

030024

研究负责人邮政编码:

Study leader's postcode:

030024

申请人所在单位:

山西省人民医院

Applicant's institution:

Shanxi Provincial People's Hospital

是否获伦理委员会批准:

Approved by ethic committee:

伦理委员会批件文号:

Approved No. of ethic committee:

(2024)省医科伦审字第138号

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件

批准本研究的伦理委员会名称:

山西省人民医院伦理委员会

Name of the ethic committee:

Shanxi Provincial People's Hospital Ethics Committee

伦理委员会批准日期:

Date of approved by ethic committee:

2024/3/5 0:00:00

伦理委员会联系人:

裴晓燕

Contact Name of the ethic committee:

Xiaoyan Pei

伦理委员会联系地址:

山西省太原市迎泽区双塔寺街29号

Contact Address of the ethic committee:

29 Shuangtasi Street, Yingze Distrcit, Taiyuan, Shanxi

伦理委员会联系人电话:

Contact phone of the ethic committee:

03514960060

伦理委员会联系人邮箱:

Contact email of the ethic committee:

sxsrmyyllwyh@126.com

研究实施负责(组长)单位:

山西中医药大学

Primary sponsor:

Shanxi University of Traditional Chinese Medicine

研究实施负责(组长)单位地址:

山西省高校园区大学街121号

Primary sponsor's address:

121 University Street, University Park, Shanxi 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):

山西省

市(区县):

Country:

China

Province:

Shanxi Province

City:

单位(医院):

山西中医药大学

具体地址:

山西省高校园区大学街121号

Institution
hospital:

Shanxi University of Traditional Chinese Medicine

Address:

121 University Street, University Park, Shanxi Province

经费或物资来源:

国家军委

Source(s) of funding:

State Military Commission

研究疾病:

脑卒中

研究疾病代码:

Target disease:

stroke

Target disease code:

研究类型:

Study type:

干预性研究

Interventional study

研究设计:

Study design:

随机平行对照

randomized controlled trial(parallel group design)

研究所处阶段:

Study phase:

上市后药物

Post-marketing clinical trial

研究目的:

探讨消栓肠溶胶囊治疗脑梗死(气虚血瘀证)的临床疗效

Objectives of Study:

To investigate the clinical effect of Xiaoshuan Chang-sol capsule in treating cerebral infarction (Qi deficiency and blood stasis syndrome)

药物成份或治疗方案详述:

Description for medicine or protocol of treatment in detail:

纳入标准:

下列各项均需满足。 ①符合诊断标准; ②发病7天内的; ③4≤NIHSS评分≤15,35≤年龄≤75周岁; ④TOAST分型为动脉粥样硬化性; ⑤患者或家属自愿签署知情同意书者; ⑥无严重并发症者; ⑦首次发病或既往卒中病史发病未留下肢体瘫痪等后遗症者; ⑧对本研究具有良好的依从性者。

Inclusion criteria

1. Patients who meet the diagnosis of acute cerebral infarction and are confirmed by CT or MRI; 2. NIHSS score: 4-15 (including 4 and 15 points); 3. Patients aged between 35 and 75 years; 4. Onset time within 7 days; 5. Patients with stable vital signs, clear consciousness and no serious complications; 6. Patients with first onset or previous history of stroke without limb paralysis and other sequelae; 7. Good compliance with this study; 8. Patients or family members sign informed consent.

排除标准:

满足任意一项即可。 ①TOAST分型中除动脉粥样硬化性以外的其他原因引起脑梗死患者; ②进展性脑梗死或反复多次发病的脑梗死患者; ③合并有严重的心血管疾病、肝肾脏器功能不全、呼吸系统疾病患者; ④有出血性疾病或精神疾病; ⑤妊娠和哺乳期妇女; ⑥本次住院接受溶栓治疗者或机械取栓者; ⑦伴认知、听力等功能障碍不能够配合评定的患者; ⑧近 90 天内参加过其他临床试验者。

Exclusion criteria:

1.In the TOAST classification, patients with cerebral infarction caused by other causes other than atherosclerosis; 2. Patients with progressive cerebral infarction or recurrent recurrent cerebral infarction; 3. Patients with severe cardiovascular diseases, liver and kidney dysfunction, and respiratory diseases; 4. Hemorrhagic disease; 5. Pregnant and lactating patients; 6.Patients who received thrombolytic therapy or mechanical thrombectomy in this hospital; 7. Patients with hearing and other dysfunction who cannot cooperate with the assessment; 8. Participated in other clinical trials within the last 90 days.

研究实施时间:

Study execute time:

From 2021-04-01

To      2022-10-30

征募观察对象时间:

Recruiting time:

From 2021-06-01

To      2022-07-31

干预措施:

Interventions:

组别:

对照组

样本量:

100

Group:

control group

Sample size:

干预措施:

基础治疗

干预措施代码:

Intervention:

basic treatment

Intervention code:

组别:

试验组

样本量:

100

Group:

treatment group

Sample size:

干预措施:

基础治疗+消栓肠溶胶囊

干预措施代码:

Intervention:

basic treatment+Xiaoshuan enteric-soluble capsule

Intervention code:

样本总量 Total sample size : 200

研究实施地点:

Countries of recruitment
and research settings:

国家:

中国

省(直辖市):

山西省

市(区县):

太原市

Country:

China

Province:

Shanxi Province

City:

Taiyuan City

单位(医院):

山西省人民医院

单位级别:

三级甲等

Institution/hospital:

Shanxi Provincial People's Hospital

Level of the institution:

Third class first class

测量指标:

Outcomes:

指标中文名:

mRS

指标类型:

主要指标

Outcome:

mRS

Type:

Primary indicator

测量时间点:

14d, 90d,

测量方法:

Measure time point of outcome:

14d, 90d,

Measure method:

指标中文名:

NIHSS 评分、日常生活活动量表、Hachinski缺血量表、Barthel 指数、中医症候量表、西医疗效量表

指标类型:

主要指标

Outcome:

NIHSS,ADL, HIS,BI. TCM syndrome score,Western medicine efficacy scale

Type:

Primary indicator

测量时间点:

0d,14d,30d,90d,

测量方法:

Measure time point of outcome:

0d,14d,30d,90d,

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

VEGF,BDNP

组织:

Sample Name:

VEGF,BDNP

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:

结束

Completed

年龄范围:

最小 35
Min age years
最大 75
Max age years

Recruiting status:

Participant age:

性别:

Gender:

男女均可

Both

随机方法(请说明由何人用什么方法产生随机序列):

温春丽利用SPSS软件产生随机数字,然后根据随机数字的大小进行排序和分组。

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

Chunli Wen generated the random allocation sequence,SPSS software was used to generate randomized numbers, and then sorted and grouped according to the size of the randomized numbers.

盲法:

双盲(参与者和研究者未知)

Blinding:

Participants and researcher were masked to the treatment.

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):

中医药防治脑卒中诊疗大数据采集分析云平台 https://sxzxyzzlm.tall.wiki/

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

Cloud platform for big data collection and analysis of TCM prevention and treatment of stroke https://sxzxyzzlm.tall.wiki/

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:

电子采集和管理系统

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

Electronic Data Capture

数据管理委员会:

Data Managemen Committee:

No

研究计划书或研究结果报告发表信息
(杂志名称、期、卷、页,时间;或网址):

Publication information of the protocol/research results report
(name of the journal, volume, issue, pages, time; or website):

国际传统医学临床试验注册平台 京ICP备07032215号-5 提示:推荐使用IE8.0以上版本 宽屏显示分辨率下使用系统