ChiCTR2000034646 版本V1.3 版本创建时间2020/07/21 00:48:33 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:

ChiCTR2000034646 

最近更新日期:

Date of Last Refreshed on:

2020-07-13 09:50:11 

注册时间:

Date of Registration:

2020-07-13 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

间歇性禁食对代谢性疾病血液相关指标及肠道菌群影响的研究

Public title:

Study on the effects of intermittent fasting on blood related parameters and gut microbiota in metabolic disease

注册题目简写:

English Acronym:

研究课题的正式科学名称:

间歇性禁食对代谢性疾病血液相关指标及肠道菌群影响的研究

Scientific title:

Study on the effects of intermittent fasting on blood related parameters and gut microbiota in metabolic disease

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:

苏君鸿 

研究负责人:

苏君鸿 

Applicant:

Junhong Su 

Study leader:

Junhong Su 

申请注册联系人电话:

Applicant telephone:

+86 13529225921

研究负责人电话:

Study leader's
telephone:

+86 13529225921

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:

j.su@kust.edu.cn

研究负责人电子邮件:

Study leader's E-mail:

j.su@kust.edu.cn

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:

云南省昆明市呈贡区景明南路727号

研究负责人通讯地址:

云南省昆明市呈贡区景明南路727号

Applicant address:

727 South Jingming Road, Chenggong District, Kunming, Yunnan, China

Study leader's address:

727 South Jingming Road, Chenggong District, Kunming, Yunnan, China

申请注册联系人邮政编码:

Applicant postcode:

650500

研究负责人邮政编码:

Study leader's postcode:

650500

申请人所在单位:

昆明理工大学医学院

Applicant's institution:

Medical School of Kunming University of Science and Technology

研究负责人所在单位:

昆明理工大学医学院

Affiliation of the Leader:

Medical School of Kunming University of Science and Technology

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:

XBMZ-YX-2016001

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:

西北民族大学医学伦理委员会

Name of the ethic committee:

Ethic committee of Northwest Minzu University

伦理委员会批准日期:

Date of approved by ethic committee:

2020-05-15 00:00:00

伦理委员会联系人:

寇炜

Contact Name of the ethic committee:

Wei Kou

伦理委员会联系地址:

甘肃省兰州市西北新村1 号, 730030

Contact Address of the ethic committee:

1 Northwest New Village, Lanzhou, Gansu, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 0931-2938152

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:

西北民族大学

Primary sponsor:

Northwest Minzu University

研究实施负责(组长)单位地址:

甘肃省兰州市西北新村1 号, 730030

Primary sponsor's address:

1 Northwest New Village, Lanzhou, Gansu, 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):

青海

市(区县):

Country:

China

Province:

Qinghai

City:

单位(医院):

青海省第五人民医院

具体地址:

青海省西宁市城东区南山东路166号

Institution
hospital:

The fifth people's hospital of Qinghai province

Address:

166 East Nanshan Road, Xining, Qinghai

国家:

中国

省(直辖市):

云南

市(区县):

Country:

China

Province:

Yunnan

City:

单位(医院):

昆明理工大学医学院

具体地址:

云南省昆明市呈贡区景明南路727号

Institution
hospital:

Medical School of Kunming University of Science and Technology

Address:

727 South Jingming Road, Chenggong District, Kunming

经费或物资来源:

西北民族大学

Source(s) of funding:

Northwest Minzu University

研究疾病:

代谢性疾病  

Target disease:

Metabolic disease

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:

其它 

Study phase:

N/A

研究设计:

单臂 

Study design:

Single arm 

研究目的:

观察间歇性禁食对代谢性疾病(肥胖,糖尿病,高血压)相关血液指标和肠道菌群的影响。  

Objectives of Study:

To observe the effects of intermittent fasting on disease-related blood parameters and gut microbiota in metabolic disease (Obesity, type 2 diabetes and hypertension).

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. 成年,性别不限;
2. 肥胖组标准: BMI大于等于28且无心血管疾病。
3. 糖尿病组标准:符合世界卫生组织(WHO)1999年颁布的糖尿病诊断标准的2型糖尿病患者且BMI大于18.5;
4. 高血压组标准:符合高血压诊断标准。
5. 能够理解本研究的程序和方法,愿意严格遵守试验方案完成本试验并自愿签署知情同意书。

Inclusion criteria

1. Adult;
2. Obesity: BMI greater than 28 & No diagostic of cardiovascular disease;
3. Type 2 diabetes: Type 2 diabetes patients who meet the diagnostic criteria for diabetes issued by the World Health Organization (WHO) in 1999 & BMI greater than 18.5;
4. Hypertension: meet the diagnostic criteria of hypertension;
5. Can understand the procedures and methods of this study, willing to strictly abide by the clinical trial protocol to complete this trial, and voluntarily sign an informed consent.

排除标准:

1. 研究前至少1月内服用抗生素;
2. 未签署知情同意书;
3. 其他慢性病(消化道系统疾病,免疫性疾病,呼吸系统疾病,心脏疾病,神经系统疾病,肿瘤);
4. BMI不符合;
5. 孕妇或备孕期;
6. 有重度低血糖发作病史(如低血糖引起嗜睡、意识障碍、胡言乱语、甚至昏迷者);
7. 资料不全的患者。
8. 参与过禁食试验的。

Exclusion criteria:

1. Antiboiotic use one month before the study;
2. Failed to provide informed consent form;
3. Other chronic disease (gastrointestinal disease, autoimmune disease, respiratory disease, heart disease, nervous system diseases, cancer)
4. Out of the defined MBI range;
5. Pregnant and lactating women;
6. Have a history of severe hypoglycemia episodes (such as sleepiness caused by hypoglycemia, unconsciousness, nonsense, and even coma);
7. Patients have no complete datas.
8. Previous participation in intermittent fasting intervention.

研究实施时间:

Study execute time:

From 2016-05-01 00:00:00 To 2021-05-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2016-05-01 00:00:00 To 2021-05-01 00:00:00

干预措施:

Interventions:

组别:

A

样本量:

50

Group:

A

Sample size:

干预措施:

间歇性禁食+肥胖

干预措施代码:

Intervention:

Intermittent fasting+obesity

Intervention code:

组别:

B

样本量:

50

Group:

B

Sample size:

干预措施:

间歇性禁食+糖尿病

干预措施代码:

Intervention:

Intermittent fasting+type 2 diabetes

Intervention code:

组别:

C1

样本量:

50

Group:

C1

Sample size:

干预措施:

间歇性禁食+高血压

干预措施代码:

Intervention:

Intermittent fasting (4wks)+hypertension

Intervention code:

组别:

C2

样本量:

50

Group:

C2

Sample size:

干预措施:

间歇性禁食(10wks)+高血压

干预措施代码:

Intervention:

Intermittent fasting (10wks)+hypertension

Intervention code:

组别:

D

样本量:

100

Group:

D

Sample size:

干预措施:

间歇性禁食+健康

干预措施代码:

Intervention:

Intermittent fasting+health

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

青海 

市(区县):

 

Country:

China

Province:

Qinghai

City:

单位(医院):

青海省第五人民医院 

单位级别:

三级 

Institution
hospital:

The fifth people's hospital of Qinghai Provience

Level of the institution:

Tertiary hospital

国家:

中国

省(直辖市):

甘肃 

市(区县):

 

Country:

China

Province:

Gansu

City:

单位(医院):

临夏州人民医院 

单位级别:

三级 

Institution
hospital:

The Peoples's Hospital of Linxia

Level of the institution:

Tertiary hospital

测量指标:

Outcomes:

指标中文名:

肠道菌群

指标类型:

主要指标

Outcome:

Gut microbiota

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血液指标

指标类型:

次要指标

Outcome:

Blood parameters

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

身体成分

指标类型:

次要指标

Outcome:

Body composition

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

饮食

指标类型:

次要指标

Outcome:

Food intake

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血压

指标类型:

主要指标

Outcome:

Blood pressure

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

基本信息

指标类型:

次要指标

Outcome:

Basic characteristics

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:

粪便

组织:

Sample Name:

Feces

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 sample

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 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):

不适用

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

N/A

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:

N/A

Blinding:

N/A

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):

发表文章形式; ResMan

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

Publish; ResMan

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:

病例记录表(Excel)

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

Case Record Form, CRF(Excel)

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2020-07-13 09:24:39