基于同步TMS-EEG精准诊治抑郁症的研究

注册号:

Registration number:

ChiCTR1800019001 

最近更新日期:

Date of Last Refreshed on:

2018-10-20 22:47:00 

注册时间:

Date of Registration:

2018-10-20 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

基于同步TMS-EEG精准诊治抑郁症的研究

Public title:

Study on accurate diagnosis and treatment of depression by using the combination of TMS-EEG

注册题目简写:

English Acronym:

研究课题的正式科学名称:

基于同步TMS-EEG精准诊治抑郁症的研究

Scientific title:

Study on accurate diagnosis and treatment of depression by using the combination of TMS-EEG

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:

任惠霞 

研究负责人:

郭毅 

Applicant:

Ren Huixia 

Study leader:

Guo Yi 

申请注册联系人电话:

Applicant telephone:

+86 13925180902

研究负责人电话:

Study leader's
telephone:

+86 13902978692

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:

shengji054@163.com

研究负责人电子邮件:

Study leader's E-mail:

xuanyi_guo@163.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:

广东省深圳市罗湖区东门北路1017号深圳市人民医院

研究负责人通讯地址:

广东省深圳市罗湖区东门北路1017号深圳市人民医院

Applicant address:

1017 North Dongmen Road, Luohu District, Shenzhen, Guangdong, China

Study leader's address:

1017 North Dongmen Road, Luohu District, Shenzhen, Guangdong, China

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:

深圳市人民医院

Applicant's institution:

Shenzhen People's Hospital

研究负责人所在单位:

深圳市人民医院

Affiliation of the Leader:

Shenzhen People's Hospital

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:

LL-KT-2018-038

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:

深圳市人民医院医学伦理委员会

Name of the ethic committee:

Shenzhen People's Hospital Medical Ethics Committee

伦理委员会批准日期:

Date of approved by ethic committee:

1990-01-01 00:00:00

伦理委员会联系人:

郑雪芬

Contact Name of the ethic committee:

Xuefen_Zheng

伦理委员会联系地址:

广东省深圳市罗湖区东门北路1017号深圳市人民医院3号楼GCP办公室

Contact Address of the ethic committee:

3 Building GCP Office, 1017 North Dongmen Road, Luohu District, Shenzhen, Guangdong, China

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:

深圳市人民医院

Primary sponsor:

Shenzhen People's Hospital

研究实施负责(组长)单位地址:

广东省深圳市罗湖区东门北路1017号深圳市人民医院

Primary sponsor's address:

1017 North Dongmen Road, Luohu District, Shenzhen, Guangdong, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

广东省

市(区县):

Country:

China

Province:

Guangdong

City:

单位(医院):

深圳市人民医院

具体地址:

广东省深圳市罗湖区东门北路1017号深圳市人民医院

Institution
hospital:

Shenzhen People's Hospital

Address:

1017 North Dongmen Road, Luohu District, Shenzhen, Guangdong, China

国家:

美国

省(直辖市):

加利福利亚

市(区县):

Country:

American

Province:

California.

City:

单位(医院):

斯坦福大学

具体地址:

美国加利福利亚州斯坦福塞拉商城450号

Institution
hospital:

Stanford university

Address:

450 Serra Mall, Stanford, CA 94305

经费或物资来源:

三名工程

Source(s) of funding:

Sanming Project

研究疾病:

抑郁症  

Target disease:

Depression

研究疾病代码:

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

诊断试验新技术临床试验 

Study phase:

Diagnostic New Technique Clincal Study

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

本项目中,我们将使用单次TMS合并脑电图( spTMS-EEG) 作为主要实验工具记录抑郁症病人对单脉冲 TMS 的响应,根据作为靶点的 p200 电位信息个体优化 rTMS 刺激参数,从而实现精准化治疗。  

Objectives of Study:

In this project, we will use a single TMS combined with electroencephalogram (spTMS-EEG) as the primary experimental tool to record the response of a depressed patient, and optimize the rTMS stimulation parameters based on the p200 potential information as a target. Accurate clinical treatment.

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:

1)存在不稳定的健康状况;
2)现存在或历史有过任何神经疾病紊乱,如脑卒中、癫痫、肿瘤、脑出血或者多发性硬化等;
3)孕妇或正在哺乳期。

Exclusion criteria:

1. Any unstable medical condition;
2. Any current or history of neurological disorders, such as stroke, seizure, tumor, hemorrhage, multiple sclerosis, etc .;
3. Currently pregnant or breastfeeding.

研究实施时间:

Study execute time:

From 2017-09-18 00:00:00 To 2020-10-18 00:00:00  

征募观察对象时间:

Recruiting time:

From 2018-09-10 00:00:00 To 2018-10-19 00:00:00

干预措施:

Interventions:

组别:

低频组

样本量:

30

Group:

Low-frequency Group

Sample size:

干预措施:

右侧DLPFC 1HZ rTMS

干预措施代码:

Intervention:

Right DLPFC 1HZ rTMS

Intervention code:

组别:

高频组

样本量:

30

Group:

High-frequency Group

Sample size:

干预措施:

左侧DLPFC, 10HZ rTMS

干预措施代码:

Intervention:

Left DLPFC, 10HZ rTMS

Intervention code:

组别:

健康对照

样本量:

30

Group:

health control

Sample size:

干预措施:

N/A

干预措施代码:

Intervention:

N/A

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

广东省 

市(区县):

 

Country:

China

Province:

Guangdong

City:

单位(医院):

深圳市人民医院 

单位级别:

三级甲等医院 

Institution
hospital:

Shenzhen People's Hospital

Level of the institution:

Tertiary A Hospital

测量指标:

Outcomes:

指标中文名:

神经量表评分

指标类型:

主要指标

Outcome:

Neurological scale

Type:

Primary 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:

N/A

组织:

Sample Name:

N/A

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:

Recruiting status:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 55 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):

实验采取随机双盲方式,由脑电数据采集人员以6位患者位单元,随机生成高频或低频rTMS治疗组

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

Randomized double-blind experimental mode taken by the EEG data acquisition unit 6 bits patients randomly generates high or low frequency rTMS treatment group

是否公开试验完成后的统计结果:

Calculated Results after the Study Completed public access:

不公开/Private

盲法:

未说明

Blinding:

Not stated

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个月内以论文的形式公开

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

as the paper format within six months after trial complete

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:

电子化数据采集: 电子数据采集(Electronic Data Capture, EDC)是一种基于计算机网络的用于临床试验数据采集的技术,通过软件、硬件、标准操作程序和人员配置的有机结合,以电子化的形式直接采集和传递临床数据。 管理: 采集的数据经上传至Box云系统,由合作方斯坦福人员下载并处理。数据采集方另外将原始数据保存至移动硬盘并刻录光盘,并存档。

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

Electronic data collection: Electronic Data Capture (EDC) is a computer network-based technology for clinical trial data collection. It is directly collected and transmitted electronically through software, hardware, standard operating procedures and staffing. Clinical data. management: The collected data is uploaded to the Box cloud system and downloaded and processed by the Stanford partner . The data collector additionally saves the original data to the mobile hard disk and burns the disc to archives it.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2018-10-20 22:47:00