痛风性关节炎湿证的临床队列构建及疗效评价研究

注册号:

Registration number:

ITMCTR2100004238

最近更新日期:

Date of Last Refreshed on:

2020-10-11

注册时间:

Date of Registration:

2020-10-11

注册号状态:

Registration Status:

预注册

Prospective registration

注册题目:

痛风性关节炎湿证的临床队列构建及疗效评价研究

Public title:

Clinical cohort construction and efficacy evaluation of gouty arthritis with dampness syndrome

注册题目简写:

English Acronym:

研究课题的正式科学名称:

痛风性关节炎湿证的临床队列构建及疗效评价研究

Scientific title:

Clinical cohort construction and efficacy evaluation of gouty arthritis with dampness syndrome

研究课题的正式科学名称简写:

Scientific title acronym:

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:

ChiCTR2000038969 ; ChiMCTR2100004238

申请注册联系人:

张晓琳

研究负责人:

黄闰月

Applicant:

Zhang Xiaolin

Study leader:

Huang Runyue

申请注册联系人电话:

Applicant telephone:

+86 15692019934

研究负责人电话:

Study leader's telephone:

+86 15889932190

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:

zhangxxiaolyx@126.com

研究负责人电子邮件:

Study leader's E-mail:

ryhuang@gzucm.edu.cn

申请单位网址(自愿提供):

Study leader's 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:

广州市白云区机场路12号广州中医药大学新宿舍楼

研究负责人通讯地址:

中国广东省广州市番禺区大学城

Applicant address:

New Dormitory Building of Guangzhou University of Traditional Chinese Medicine, 12 Airport Road, Baiyun District, Guangzhou, Guangdong, China

Study leader's address:

University Town, Panyu District, Guangzhou, 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:

广州中医药大学第二临床医学院

Applicant's institution:

The Second Clinical College of Guangzhou University of Chinese Medicine

是否获伦理委员会批准:

Approved by ethic committee:

伦理委员会批件文号:

Approved No. of ethic committee:

BF2020-193-01

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件

批准本研究的伦理委员会名称:

广东省中医院伦理委员会

Name of the ethic committee:

Ethics Committee of Guangdong Provincial Hospital of Chinese Medicine

伦理委员会批准日期:

Date of approved by ethic committee:

2020/9/2 0:00:00

伦理委员会联系人:

李晓彦

Contact Name of the ethic committee:

Xiaoyan Li

伦理委员会联系地址:

广东省广州市越秀区大德路111号广东省中医院研修楼1912房

Contact Address of the ethic committee:

Room 1912, 111 Dade Road, Yuexiu District, Guangzhou, 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:

广东省中医院

Primary sponsor:

Guangdong Provincial Hospital of Chinese Medicine

研究实施负责(组长)单位地址:

广州市越秀区大德路111号

Primary sponsor's address:

111 Dade Road, Yuexiu District, Guangzhou, 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

市(区县):

广州

Country:

China

Province:

Guangdong

City:

Guangzhou

单位(医院):

广东省中医院

具体地址:

越秀区大德路111号

Institution
hospital:

Guangdong Provincial Hospital of Chinese Medicine

Address:

111 Dade Road, Yuexiu District

经费或物资来源:

省部共建中医湿证国家重点实验室(广州中医药大学第二附属医院)

Source(s) of funding:

Laboratory of Dampness Syndrome of Chinese Medicine (The Second Affiliated Hospital of Guangzhou University of Chinese Medicine)

研究疾病:

痛风性关节炎

研究疾病代码:

Target disease:

Gouty arthritis

Target disease code:

研究类型:

Study type:

观察性研究

Observational study

研究设计:

Study design:

连续入组

Sequential

研究所处阶段:

Study phase:

探索性研究/预试验

Pilot clinical trial

研究目的:

观察祛湿法干预后对痛风性关节炎复发率的影响,并时构建痛风性关节炎湿证生物样本库,开展从湿论治痛风性关节炎的效应机制研究。

Objectives of Study:

To observe the influence of intervention on the recurrence rate of gouty arthritis by removing damp, and to construct the wet-syndrome biological sample library of gouty arthritis in order to research the effect mechanism of treating gouty arthritis based on wet-theory by using multi-group and bioinformatics methods.

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2015年ACR/EULAR痛风性关节炎诊断标准。*评分≥8分者可诊断为痛风。 (2)自愿参加病例注册登记研究,签署知情同意

Inclusion criteria

1. Patients meeting the 2015 ACR / EULAR diagnostic criteria for gouty arthritis. *Gout can be diagnosed if the score is more than 8; 2. Patients who voluntarily participate in case registration study and sign informed consent.

排除标准:

(1)继发性痛风(潜在疾病所致或药物如阿司匹林、环孢素、利尿剂等造成痛风者); (2)妊娠或哺乳期的妇女; (3)合并严重心脑血管疾病、肝、肾、恶性肿瘤、造血系统及精神疾病者。

Exclusion criteria:

1. Patients with secondary gout (Gout Caused by potential diseases or drugs such as aspirin, cyclosporine, diuretics, etc.); 2. Pregnant or lactating women; 3. Patients with severe cardiovascular and cerebrovascular diseases, liver, kidney, malignant tumors, hematopoietic system and mental diseases.

研究实施时间:

Study execute time:

From 2020-08-01

To      2023-12-31

征募观察对象时间:

Recruiting time:

From 2020-10-01

To      2022-12-31

干预措施:

Interventions:

组别:

case series

样本量:

200

Group:

case series

Sample size:

干预措施:

中药汤剂

干预措施代码:

Intervention:

traditional chinese medicine decoction

Intervention code:

样本总量 Total sample size : 200

研究实施地点:

Countries of recruitment
and research settings:

国家:

中国

省(直辖市):

广东

市(区县):

广州

Country:

China

Province:

Guangdong

City:

Guangzhou

单位(医院):

广东省中医院

单位级别:

三级甲等

Institution/hospital:

Guangdong Provincial Hospital of Chinese Medicine

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

肾小球滤过率

指标类型:

主要指标

Outcome:

eGFR

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

肌酐

指标类型:

主要指标

Outcome:

Cr

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

安全性

指标类型:

次要指标

Outcome:

medication safety

Type:

Secondary indicator

测量时间点:

测量方法:

肝功能、肾功能、心酶

Measure time point of outcome:

Measure method:

指标中文名:

尿酸

指标类型:

主要指标

Outcome:

UA

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

甘油三酯

指标类型:

次要指标

Outcome:

TG

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

C反应蛋白

指标类型:

主要指标

Outcome:

CRP

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血糖

指标类型:

次要指标

Outcome:

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:

总胆固醇

指标类型:

次要指标

Outcome:

TC

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

关节症状及体征

指标类型:

次要指标

Outcome:

Joint symptoms and signs

Type:

Secondary indicator

测量时间点:

测量方法:

受累关节分布及症状、发作次数

Measure time point of outcome:

Measure method:

指标中文名:

血沉

指标类型:

主要指标

Outcome:

ESR

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

全身症状及体征

指标类型:

次要指标

Outcome:

General symptoms and signs

Type:

Secondary indicator

测量时间点:

测量方法:

CRP、患者对疾病总体状况VAS评分及焦虑自评表SAS、抑郁自评量表SDS

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

尿液

组织:

Sample Name:

urine

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:

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:

静脉血

Sample Name:

Blood

Tissue:

blood from vein

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:

正在进行

Recruiting

年龄范围:

最小 18
Min age years
最大 70
Max age years

Recruiting status:

Participant age:

性别:

Gender:

男女均可

Both

随机方法(请说明由何人用什么方法产生随机序列):

无随机

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

Non-randomization.

盲法:

N/A

Blinding:

N/A

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):

试验完成后6个月内公开原始数据,原始数据上传至中国临床试验注册中心

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

The original data disclosure time is within six months of the completion of the test and the data will uploaded to the China Clinical Trial Registration Center.

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:

使用纸质版CRF表及ResMan软件。

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

Via paper version of CRF and ResMan software.

数据管理委员会:

Data Managemen Committee:

Yes

研究计划书或研究结果报告发表信息
(杂志名称、期、卷、页,时间;或网址):

Publication information of the protocol/research results report
(name of the journal, volume, issue, pages, time; or website):

国际传统医学临床试验注册平台 京ICP备07032215号-5 提示:推荐使用IE8.0以上版本 宽屏显示分辨率下使用系统