|
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: |
|
||||||||||||||||||||||
|
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: |
从 From 2021-12-01 00:00:00至 To 2023-06-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2021-12-01 00:00:00 至 To 2022-12-30 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
正在进行 Recruiting |
年龄范围: Participant age: |
|
||||||
|
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
|
|
|
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 |