ChiCTR2200059183 版本V1.1 版本创建时间2023/01/20 16:51:07 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:

ChiCTR2200059183 

最近更新日期:

Date of Last Refreshed on:

2023-01-20 16:36:26 

注册时间:

Date of Registration:

2022-04-26 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

肠道菌群调控TLR4/NF-kB通路影响利培酮抗精神分裂症效应的机制及应用研究

Public title:

Mechanism and application of intestinal flora regulating TLR4 / NF KB pathway on the anti schizophrenic effect of risperidone

注册题目简写:

English Acronym:

研究课题的正式科学名称:

肠道菌群调控TLR4/NF-kB通路影响利培酮抗精神分裂症效应的机制及应用研究

Scientific title:

Mechanism and application of intestinal flora regulating TLR4 / NF KB pathway on the anti schizophrenic effect of risperidone

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:

朱浩浩 

研究负责人:

杜志强 

Applicant:

Zhu Haohao 

Study leader:

Du Zhiqiang 

申请注册联系人电话:

Applicant telephone:

+86 13373614175

研究负责人电话:

Study leader's
telephone:

+86 13358111376

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:

zhux58@163.com

研究负责人电子邮件:

Study leader's E-mail:

duoduo1137@163.com

申请单位网址(自愿提供):

Applicant website(voluntary supply):

http://www.wuximhc.com/

研究负责人网址(自愿提供):

Study leader's website(voluntary supply):

http://www.wuximhc.com/

申请注册联系人通讯地址:

江苏省无锡市钱荣路156号

研究负责人通讯地址:

江苏省无锡市钱荣路156号

Applicant address:

156 Qianrong Road, Wuxi, Jiangsu

Study leader's address:

156 Qianrong Road, Wuxi, Jiangsu

申请注册联系人邮政编码:

Applicant postcode:

214151

研究负责人邮政编码:

Study leader's postcode:

214151

申请人所在单位:

无锡市精神卫生中心

Applicant's institution:

Wuxi Mental Health Center

研究负责人所在单位:

无锡市精神卫生中心

Affiliation of the Leader:

Wuxi Mental Health Center

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:

WXMHCIRB2021LLky127

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:

无锡市精神卫生中心伦理委员会

Name of the ethic committee:

Wuxi Mental Health Center Ethics Committee

伦理委员会批准日期:

Date of approved by ethic committee:

2021-10-14 00:00:00

伦理委员会联系人:

计樱莹

Contact Name of the ethic committee:

Ji Yingying

伦理委员会联系地址:

江苏省无锡市钱荣路156号

Contact Address of the ethic committee:

156 Qianrong Road, Wuxi, Jiangsu

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 18936070211

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:

无锡市精神卫生中心

Primary sponsor:

Wuxi Mental Health Center

研究实施负责(组长)单位地址:

江苏省无锡市钱荣路156号

Primary sponsor's address:

156 Qianrong Road, Wuxi, Jiangsu

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国·

省(直辖市):

江苏

市(区县):

无锡

Country:

China

Province:

Jiangsu

City:

Wuxi

单位(医院):

无锡市精神卫生中心

具体地址:

钱荣路156号

Institution
hospital:

Wuxi Mental Health Center

Address:

156 Qianrong Road

经费或物资来源:

无锡市卫生健康委员会

Source(s) of funding:

Wuxi Health Commission

研究疾病:

抑郁症  

Target disease:

Major depression disorder

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:

探索性研究/预试验 

Study phase:

0

研究设计:

析因分组(即根据危险因素或暴露因素分组) 

Study design:

Factorial 

研究目的:

(1)明确肠道菌群及其代谢物多样性差异与RIP抗SCZ疗效的相关性; (2)明确肠道菌群通过代谢途径调控TLR4/NF-κB/TNF-α通路影响RIP抗SCZ疗效的分子机制。  

Objectives of Study:

(1) To clarify the correlation between the diversity of intestinal flora and its metabolites and the anti SCZ efficacy of rip; (2) It is clear that intestinal flora regulates TLR4 / NF through metabolic pathway- κ B/TNF- α The molecular mechanism of the pathway affecting the anti SCZ efficacy of rip.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

纳入标准:汉族;符合美国精神障碍诊断与统计手册第 4 版 (Diagnostic and Statistical Manual of Mental Disorders,Fourth Edition,DSM -IV) 关于SCZ的临床诊断标准;年龄 18~45岁,性别不限;阳性与阴性症状量表(Positive and Negative Symptom Scale,PANSS)总分≥60分。

Inclusion criteria

Inclusion criteria: Han nationality; Comply with the clinical diagnostic criteria of SCZ in the diagnostic and Statistical Manual of mental disorders, Fourth Edition (DSM-IV); Age 18-45 years old, gender unlimited; The total score of positive and negative symptom scale (PANSS) is ≥ 60.

排除标准:

伴有其他的精神类疾病或既往有其他的精神类疾病患者;既往有脑器质性病变或脑部受到过严重外伤者;伴有严重的心、肝、肾功能不全,代谢性疾病以及其他严重性身体疾病者;处于妊娠或哺乳期的妇女;近一个月内连续服用或使用过抗生素(或)微生态调节剂者;实验室常规检查(如肝功能、血常规和尿常规等)异常者;3个月内参加过另一个临床研究;患有严重的不稳定的躯体疾病者,已确诊的糖尿病、甲状腺疾病、高血压病等。

Exclusion criteria:

Patients with other mental diseases or previous mental diseases; Previous organic brain lesions or severe brain trauma; Accompanied by severe heart, liver and kidney dysfunction, metabolic diseases and other serious physical diseases; Pregnant or lactating women; Those who have taken or used antibiotics (or microecological regulators) continuously in the past month; Patients with abnormal liver function and routine laboratory examination; Participated in another clinical study within 3 months; Those who suffer from severe unstable physical diseases are diagnosed as diabetes, thyroid disease, hypertension, etc.

研究实施时间:

Study execute time:

From 2022-01-01 00:00:00 To 2023-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-04-30 00:00:00 To 2023-12-31 00:00:00

干预措施:

Interventions:

组别:

连续入组

样本量:

100

Group:

case series

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):

江苏 

市(区县):

无锡 

Country:

China

Province:

Jiangsu

City:

Wuxi

单位(医院):

无锡市精神卫生中心 

单位级别:

三甲 

Institution
hospital:

Wuxi Mental Health Center

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

肠道菌群

指标类型:

主要指标

Outcome:

Intestinal flora

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

炎症因子

指标类型:

主要指标

Outcome:

Inflammatory factor

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:

粪便

组织:

Sample Name:

Faeces

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

标本中文名:

血液

组织:

Sample Name:

Blood

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:

尚未开始

Not yet 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):

根据治疗效果分为对照组(无效)及观察组(有效)

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

According to the treatment effect, they were divided into control group (ineffective) and observation group (effective)

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:

no

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

否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):

联系主要负责人获得

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

Contact the principal to obtain

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, EDC

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2022-04-26 05:21:40