ChiCTR2100054008 版本V1.0 版本创建时间2022/05/30 21:01:04 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:

ChiCTR2100054008 

最近更新日期:

Date of Last Refreshed on:

2021-12-06 09:28:11 

注册时间:

Date of Registration:

2021-12-06 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

请于伦理委员会批准后才开始征募参试者,并与我们联系上传伦理批件。 迷走神经磁刺激治疗卒中后认知障碍的临床研究

Public title:

Clinical study of vagus nerve magnetic stimulation for post-stroke cognitive impairment

注册题目简写:

English Acronym:

研究课题的正式科学名称:

迷走神经磁刺激治疗卒中后认知障碍的临床研究

Scientific title:

Clinical study of vagus nerve magnetic stimulation for post-stroke cognitive impairment

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:

杨正蕾 

研究负责人:

吴青 

Applicant:

Yang Zhenglei 

Study leader:

Wu Qing 

申请注册联系人电话:

Applicant telephone:

18225519427

研究负责人电话:

Study leader's telephone:

13696238919

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:

468590589@qq.com

研究负责人电子邮件:

Study leader's E-mail:

cbyfy2017@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:

四川省南充市顺庆区茂源南路1号

研究负责人通讯地址:

四川省南充市顺庆区茂源南路1号

Applicant address:

No.1 Maoyuan South Road, Shunqing District, Nanchong City, Sichuan Province

Study leader's address:

No.1 Maoyuan South Road, Shunqing District, Nanchong City, Sichuan Province

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:

川北医学院附属医院

Applicant's institution:

Affiliated Hospital of North Sichuan Medical College

研究负责人所在单位:

Affiliation of the Leader:

是否获伦理委员会批准:

否/No

Approved by ethic committee:

No

伦理委员会批件文号:

Approved No. of ethic committee:

伦理委员会批件附件:

Approved file of Ethical Committee:

批准本研究的伦理委员会名称:

Name of the ethic committee:

伦理委员会批准日期:

Date of approved by ethic committee:

2013-08-26 00:00:00

伦理委员会联系人:

Contact Name of the ethic committee:

伦理委员会联系地址:

Contact Address of the ethic committee:

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:

川北医学院附属医院

Primary sponsor:

Affiliated Hospital of North Sichuan Medical College

研究实施负责(组长)单位地址:

四川省南充市顺庆区茂源南路1号

Primary sponsor's address:

No.1 Maoyuan South Road, Shunqing District, Nanchong City, Sichuan 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):

四川

市(区县):

南充

Country:

China

Province:

Sichuan

City:

Nanchong

单位(医院):

川北医学院附属医院

具体地址:

顺庆区茂源南路1号

Institution
hospital:

Affiliated Hospital of North Sichuan Medical College

Address:

1 Maoyuan Road South, Shunqing District

经费或物资来源:

研究生经费

Source(s) of funding:

Graduate Student Funding

Target disease:

post-stroke cognitive impairment

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:

1.通过迷走神经磁刺激对卒中后认知障碍的影响,验证迷走神经磁刺激对卒中后认知障碍的临床疗效,寻找PSCI新的有效刺激靶点。 2.探索迷走神经磁刺激改善卒中后认知障碍可能的脑网络调节机制。  

Objectives of Study:

1. To verify the clinical efficacy of vagus nerve magnetic stimulation on post-stroke cognitive impairment and to find new effective stimulation targets for PSCI through the effect of vagus nerve magnetic stimulation on post-stroke cognitive impairment. 2. To explore the possible mechanisms of brain network modulation by vagus nerve magnetic stimulation to improve post-stroke cognitive impairment.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

符合中华医学会第四次全国脑血管病学术会议修订的《各类脑血管疾病诊断要点》的诊断标准及经CT或MRI证实,诊断为缺血性或出血性卒中;首次脑卒中,病程2周-2个月内;存在认知障碍,蒙特利尔认知评估量表(Montreal cognitive assessment,MoCA)评分<26分;患者神志清楚,生命体征平稳,神经科症状无进展;无严重失语及听理解障碍,可完成记忆及认知专项检测;无精神类疾病等;入组前均需取得患者及家属同意,并签署治疗知情同意书。

Inclusion criteria

The diagnosis of ischemic or hemorrhagic stroke was confirmed by CT or MRI; first stroke, within 2 weeks-2 months; cognitive impairment, Montreal cognitive assessment scale (MoCA) score <26; clear consciousness, stable vital signs, no progression of neurological symptoms; no severe aphasia or auditory comprehension disorder, no memory and cognitive specific tests; no psychiatric disorders, etc, MoCA score <26; clear consciousness, stable vital signs, no progression of neurological symptoms; no severe aphasia and hearing comprehension impairment; no memory and cognitive specific tests; no psychiatric disorders; all patients and family members were required to give their consent and sign the informed consent form before enrollment.

排除标准:

非首次卒中;伴意识障碍;卒中前存在认知功能减退;有明显失语及听理解障碍、有严重听力或视力障碍不能配合康复治疗;有明显精神及情绪异常,影响康复治疗;有心、肺、肝、肾等重要脏器功能异常;任何影响评估及治疗的其他因素。

Exclusion criteria:

Non-first stroke; with impaired consciousness; pre-stroke cognitive impairment; significant aphasia and hearing comprehension impairment, severe hearing or visual impairment that prevents cooperation with rehabilitation; significant mental and emotional abnormalities that interfere with rehabilitation; significant organ function abnormalities such as heart, lung, liver and kidney; any other factors that affect assessment and treatment.

研究实施时间:

Study execute time:

From 2021-12-01 00:00:00 To 2023-06-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2021-12-01 00:00:00 To 2022-12-30 00:00:00  

干预措施:

Interventions:

组别:

迷走神经磁刺激组

样本量:

30

Group:

Vagus nerve magnetic stimulation group

Sample size:

干预措施:

迷走神经磁刺激

干预措施代码:

Intervention:

Vagus nerve magnetic stimulation

Intervention code:

组别:

假刺激组

样本量:

30

Group:

False stimulus group

Sample size:

干预措施:

假刺激

干预措施代码:

Intervention:

False stimulus

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

四川 

市(区县):

南充 

Country:

China 

Province:

Sichuan 

City:

Nanchong 

单位(医院):

川北医学院附属医院 

单位级别:

三级甲等 

Institution
hospital:

Affiliated Hospital of North Sichuan Medical College

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

简易精神状态量表

指标类型:

主要指标

Outcome:

Mini-Mental State Examination

Type:

Primary indicator

测量时间点:

治疗前、治疗后和治疗结束后2周

测量方法:

Measure time point of outcome:

Pre-treatment, post-treatment and 2 weeks after the end of treatment

Measure method:

指标中文名:

蒙特利尔认知评估量表

指标类型:

主要指标

Outcome:

Montreal Cognitive Assessment

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

事件相关电位P300

指标类型:

次要指标

Outcome:

Event-related potential P300

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

功能近红外光谱

指标类型:

次要指标

Outcome:

Functional near infrared spectroscopy

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

脑电图

指标类型:

次要指标

Outcome:

Electroencephalogram

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

NINDS-CNS关于VCI标准化神经心理测验的建议

指标类型:

次要指标

Outcome:

NINDS-CNS Recommendations for VCI Standardized Neuropsychological Tests

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:

组织:

Sample Name:

N/A

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:

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):

由统计中心根据电脑随机数字分组

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

According to the computer random number control by the centre of statistical

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:

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

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):

试验完成后6个月内在临床试验管理平台公开本研究全部数据

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

Within six months after the trial complete, Clinical Trial Management Public Platform

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:

使用病例记录表采集数据

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

Case Record Form, CRF

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2021-12-06 09:28:12