ChiCTR2500105892 版本V1.0 版本创建时间2025/07/14 15:02:40 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:

ChiCTR2500105892 

最近更新日期:

Date of Last Refreshed on:

2025-07-14 15:02:21 

注册时间:

Date of Registration:

2025-07-14 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

基于非线性EEG和fNIRS评估针刺对意识障碍患者促醒的影响

Public title:

The effects of acupuncture on awakening in patients with disturbance of consciousness were evaluated based on nonlinear EEG and fNIRS

注册题目简写:

English Acronym:

研究课题的正式科学名称:

基于非线性EEG和fNIRS评估针刺对意识障碍患者促醒的影响

Scientific title:

The effects of acupuncture on awakening in patients with disturbance of consciousness were evaluated based on nonlinear EEG and fNIRS

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:

黄来刚 

研究负责人:

黄来刚 

Applicant:

Laigang Huang 

Study leader:

Laigang Huang 

申请注册联系人电话:

Applicant telephone:

+86 176 6008 9943

研究负责人电话:

Study leader's
telephone:

+86 176 6008 9943

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:

1250815700@qq.com

研究负责人电子邮件:

Study leader's E-mail:

1250815700@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:

山东省济南市天桥区北园大街山东大学第二医院

研究负责人通讯地址:

山东省济南市天桥区北园大街山东大学第二医院

Applicant address:

The Second Hospital of Shandong University, Beiyuan Street, Tianqiao District, Jinan City, Shandong Province

Study leader's address:

The Second Hospital of Shandong University, Beiyuan Street, Tianqiao District, Jinan City, Shandong 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:

山东大学第二医院

Applicant's institution:

The Second Hospital of Shandong University

研究负责人所在单位:

山东大学第二医院

Affiliation of the Leader:

The Second Hospital of Shandong University

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:

KYLL2024456

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:

山东大学第二医院科研伦理委员会

Name of the ethic committee:

Research Ethics Committee of the Second Hospital of Shandong University

伦理委员会批准日期:

Date of approved by ethic committee:

2024-04-01 00:00:00

伦理委员会联系人:

徐小舟

Contact Name of the ethic committee:

Xiaozhou xu

伦理委员会联系地址:

山东省济南市天桥区北园大街山东大学第二医院

Contact Address of the ethic committee:

The Second Hospital of Shandong University, Beiyuan Street, Tianqiao District, Jinan City, Shandong Province

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 176 6008 9943

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:

山东大学第二医院

Primary sponsor:

The Second Hospital of Shandong University

研究实施负责(组长)单位地址:

山东省济南市天桥区北园大街山东大学第二医院

Primary sponsor's address:

The Second Hospital of Shandong University, Beiyuan Street, Tianqiao District, Jinan City, Shandong 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):

山东

市(区县):

Country:

China

Province:

Shandong

City:

单位(医院):

山东大学第二医院

具体地址:

山东省济南市天桥区北园大街山东大学第二医院

Institution
hospital:

The Second Hospital of Shandong University

Address:

The Second Hospital of Shandong University, Beiyuan Street, Tianqiao District, Jinan City, Shandong Province

经费或物资来源:

山东大学第二医院高原学科建设经费2万

Source(s) of funding:

The Second Hospital of Shandong University allocated 20,000 yuan for the construction of plateau discipline

研究疾病:

意识障碍  

Target disease:

Disorders of consciousness

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:

其它 

Study phase:

N/A

研究设计:

横断面 

Study design:

Cross-sectional 

研究目的:

基于非线性EEG和fNIRS评估针刺对意识障碍患者促醒的影响  

Objectives of Study:

The effects of acupuncture on awakening in patients with disturbance of consciousness were evaluated based on nonlinear EEG and fNIRS

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.符合 DOC 诊断标准,且诊断为UWS或MCS; 2.年龄 18~80 周岁; 3.可以诱发出正常脑干听觉诱发电位; 4.既往无脑损伤史; 5.患者监护人自愿参与研究,签署知情同意书。

Inclusion criteria

1.It meets DOC diagnostic criteria and is diagnosed as UWS or MCS; 2. Age 18-80 years old; 3. Can induce normal brainstem auditory evoked potential; 4. no previous history of brain injury; 5. The patient's guardian voluntarily participated in the study and signed the informed consent.

排除标准:

1.病情持续加重,活动性脑出血或颅内高压尚未控制; 2.闭锁综合征,严重脑萎缩,脑积水; 3.既往有癫痫史; 4.严重痉挛,导致肌电图伪影; 5.颅骨减压切除术或影响区域脑电图振幅的颅骨缺损患者。

Exclusion criteria:

1.The disease continues to worsen, active cerebral hemorrhage or intracranial hypertension has not been controlled; 2.Locked-in syndrome, severe cerebral atrophy, hydrocephalus; 3.Have a history of epilepsy; 4.Severe spasm, resulting in EMG artifacts; 5.Cranial decompression resection or affected regional EEG amplitude of the skull defect patients.

研究实施时间:

Study execute time:

From 2023-12-25 00:00:00 To 2026-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2023-12-25 00:00:00 To 2026-12-31 00:00:00

干预措施:

Interventions:

组别:

观察组

样本量:

29

Group:

Observation group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

山东 

市(区县):

济南 

Country:

China

Province:

Shangdong

City:

Jinan

单位(医院):

山东大学第二医院 

单位级别:

三甲 

Institution
hospital:

The Second Hospital of Shandong University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

近似熵

指标类型:

主要指标

Outcome:

ApEn

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

氧和血红蛋白

指标类型:

次要指标

Outcome:

Oxygen and hemoglobin

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:

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:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 80 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:

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

是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):

试验完成后6个月,ResMan平台 http://www.clinicaltrialecrf.org

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

Six months after the completion of the trial, the ResMan platform http://www.clinicaltrialecrf.org

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:

本研究采用专人管理病例记录表(Case Record Form, CRF)

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

In this study, Case Record Form (CRF) was administered by special personnel.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2025-07-14 15:02:21