ChiCTR1900025601 版本V1.0 版本创建时间2019/09/26 09:40:39 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:

ChiCTR1900025601 

最近更新日期:

Date of Last Refreshed on:

2019-09-02 09:22:11 

注册时间:

Date of Registration:

2019-09-02 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

丹蒌片对冠心病患者肠道菌群影响及其代谢组学研究

Public title:

Study for the effect of Danlou tablet on gut microbiota of CHD patients and its metabolomics

注册题目简写:

English Acronym:

研究课题的正式科学名称:

丹蒌片对冠心病患者肠道菌群影响及其代谢组学研究

Scientific title:

Study for the effect of Danlou tablet on gut microbiota of CHD patients and its metabolomics

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:

李玉红 

研究负责人:

李玉红 

Applicant:

Li Yuhong 

Study leader:

Li Yuhong 

申请注册联系人电话:

Applicant telephone:

+86 13352057819

研究负责人电话:

Study leader's telephone:

+86 13352057819

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:

yhltcm@126.com

研究负责人电子邮件:

Study leader's E-mail:

yhltcm@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:

天津市静海区北华南路

研究负责人通讯地址:

天津市静海区北华南路

Applicant address:

South Beibei Road, Jinghai District, Tianjin, China

Study leader's address:

South Beibei Road, Jinghai District, Tianjin, 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:

天津中医药大学

Applicant's institution:

Tianjin University of Traditional Chinese Medicine

研究负责人所在单位:

天津中医药大学

Affiliation of the Leader:

Tianjin University of Traditional Chinese Medicine

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:

黑龙江省齐齐哈尔市泰来县中医医院

Primary sponsor:

Traditional Chinese Medicine Hospital of Tailai County, Qiqihar City, Heilongjiang Province

研究实施负责(组长)单位地址:

齐齐哈尔市泰来县金源街157号

Primary sponsor's address:

57 Jinyuan Street, Tailai, Qiqihar, Heilongjiang, 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):

天津

市(区县):

Country:

China

Province:

Tianjin

City:

单位(医院):

天津中医药大学

具体地址:

天津市静海区北华南路

Institution
hospital:

Tianjin University of Traditional Chinese Medicine

Address:

South Beibei Road, Jinghai District, Tianjin

经费或物资来源:

自筹

Source(s) of funding:

self-finance

Target disease:

coronary heart disease

Target disease code:

研究类型:

基础科学研究

Study type:

Basic Science

研究所处阶段:

上市后药物 

Study phase:

4

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

观察丹蒌片对冠心病患者肠道菌群、代谢组学的影响  

Objectives of Study:

To observe the effect of Danlou tablet on gut microbiota and metabolomics of CHD patients

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

年龄在40-85岁之间;
符合稳定性冠心病诊断标准;
签订临床试验知情同意书。

Inclusion criteria

1. Aged between 40-85 years;
2. Meets the diagnostic criteria for stable coronary heart disease;
3. singed the consent form.

排除标准:

1合并先天性心脏病、风湿性心脏病、不稳定性心绞痛;
2瓣膜病、疑诊为主动脉夹层、心律失常、急性心力衰竭、中度至重度肺动脉高压及急性肺栓塞等严重心肺功能障碍;
3严重肝肾功能障碍或免疫类疾病;
4急性感染;
5实验前2周及期间使用抗生素、其他降血脂、降血糖药物及其他中成药的患者;
6非自愿、依从性差的患者;
7正在参加其他临床试验者。

Exclusion criteria:

1. Combined with Congenital heart disease, rheumatic heart disease, unstable angina pectoris;
2. Combined with Valvular disease, suspected major artery dissection, arrhythmia, acute heart failure, moderate to severe pulmonary hypertension, acute pulmonary embolism and other serious cardiopulmonary dysfunction;
3. Combined with Severe liver and kidney dysfunction, immune diseases;
4. Combined with acute infection;
5. Patients who used antibiotics, other lipid-lowering and blood-glucose lowering drugs and other Chinese medicines before 2 weeks and during the experiment;
6. Involuntary patients, poor compliance;
7. Participated in other clinical trials.

研究实施时间:

Study execute time:

From 2019-01-01 00:00:00 To 2019-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2019-09-15 00:00:00 To 2019-11-15 00:00:00  

干预措施:

Interventions:

组别:

丹蒌片与丹参川芎嗪注射液组

样本量:

30

Group:

DLT-SML

Sample size:

干预措施:

口服丹蒌片、常规静脉注射丹参川芎嗪注射液

干预措施代码:

Intervention:

Oral Danlou tablets and iv. Salvia miltiorrhiza ligustrazine injection

Intervention code:

组别:

健康对照组

样本量:

10

Group:

Health control (not randomized)

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):

黑龙江 

市(区县):

 

Country:

China 

Province:

Heilongjiang 

City:

 

单位(医院):

齐齐哈尔市泰来县中医医院 

单位级别:

二级甲等 

Institution
hospital:

Traditional Chinese Medicine Hospital of Tailai County, Qiqihar City,

Level of the institution:

Secondary A Hospital

测量指标:

Outcomes:

指标中文名:

血常规

指标类型:

副作用指标

Outcome:

blood routine examinatio

Type:

Adverse events

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

尿常规

指标类型:

副作用指标

Outcome:

routine urine test

Type:

Adverse events

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

肝肾功能

指标类型:

副作用指标

Outcome:

hepatic and renal function

Type:

Adverse events

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

不良反应

指标类型:

副作用指标

Outcome:

adverse event

Type:

Adverse events

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

终点事件

指标类型:

副作用指标

Outcome:

outcome event

Type:

Adverse events

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

白细胞介素-1β

指标类型:

主要指标

Outcome:

IL-1β

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血脂四项和血糖

指标类型:

次要指标

Outcome:

lipid panel (TG, TC, HDL-c, and LDL-c), GLU

Type:

Secondary 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(IL-6, IL-10, TNF-α)

指标类型:

次要指标

Outcome:

inflammation cytokines (IL-6, IL-10, TNF-α)

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

肠道菌群代谢产物(LPS, TMAO)

指标类型:

次要指标

Outcome:

gut-derived metabolites (LPS, TMAO) level

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

肠道菌群

指标类型:

次要指标

Outcome:

gut microbiota

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

心电图

指标类型:

副作用指标

Outcome:

ECG

Type:

Adverse events

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:

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:

标本中文名:

大便

组织:

Sample Name:

shit

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 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):

研究人员使用计算机程序(SAS 9.2)产生随机序列

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

he researchers used a computer program (SAS 9.2) to generate random sequences

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

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):

科研文章的形式公开

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

publish scientific paper

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

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

Case report form

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2019-09-02 09:22:11