过敏性紫癜肾炎患者外周血Th17/Treg细胞轴表达的相关性研究

注册号:

Registration number:

ChiCTR1900025155 

最近更新日期:

Date of Last Refreshed on:

2019-08-14 22:49:05 

注册时间:

Date of Registration:

2019-08-14 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

过敏性紫癜肾炎患者外周血Th17/Treg细胞轴表达的相关性研究

Public title:

Correlation study for expression of peripheral blood Th17/Treg cell axis in HSPN patients

注册题目简写:

English Acronym:

研究课题的正式科学名称:

过敏性紫癜肾炎患者外周血Th17/Treg细胞轴表达的相关性研究

Scientific title:

Correlation study for expression of peripheral blood Th17/Treg cell axis in HSPN patients

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:

薛雪 

研究负责人:

薛雪 

Applicant:

Xue Xue 

Study leader:

Xue Xue 

申请注册联系人电话:

Applicant telephone:

+86 13971217560

研究负责人电话:

Study leader's
telephone:

+86 13971217560

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:

xue025004138@163.com

研究负责人电子邮件:

Study leader's E-mail:

xue025004138@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:

湖北省武汉市洪山区黄家湖西路1号

研究负责人通讯地址:

湖北省武汉市洪山区黄家湖西路1号

Applicant address:

1 Huangjiahu Road West, Hongshan District, Wuhan, Hubei.

Study leader's address:

1 Huangjiahu Road West, Hongshan District, Wuhan, Hubei.

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:

湖北中医药大学

Applicant's institution:

Hubei University of Traditional Chinese Medicine

研究负责人所在单位:

湖北中医药大学

Affiliation of the Leader:

Hubei University of Traditional Chinese Medicine

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:

HBZY2019-C37-01

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:

湖北省中医院伦理委员会

Name of the ethic committee:

Ethics Committee of Hubei Provincial Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2019-07-25 00:00:00

伦理委员会联系人:

张馨

Contact Name of the ethic committee:

Xin Zhang

伦理委员会联系地址:

湖北省武汉市花园山4号

Contact Address of the ethic committee:

4 Garden Hill, Wuhan, Hubei, 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:

湖北中医药大学

Primary sponsor:

Hubei University of Traditional Chinese Medicine

研究实施负责(组长)单位地址:

湖北省武汉市洪山区黄家湖西路1号

Primary sponsor's address:

1 Huangjiahu Road West, Hongshan District, Wuhan, Hubei, 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):

湖北

市(区县):

武汉市

Country:

China

Province:

Hubei

City:

Wuhan

单位(医院):

湖北省中医院

具体地址:

花园山4号

Institution
hospital:

Hubei Provincial Hospital

Address:

4 Garden Hill

经费或物资来源:

湖北省教育厅科研项目青年项目资助

Source(s) of funding:

Hubei Provincial Department of Education Research Project (Youth Project )Funding

研究疾病:

过敏性紫癜性肾炎  

Target disease:

Henoch-Sch?nlein purpura nephritis(HSPN)

研究疾病代码:

Target disease code:

研究类型:

基础科学研究

Study type:

Basic Science

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:

探讨成人紫癜性肾炎的发病机制是否与Th17/Treg细胞轴失衡有关。  

Objectives of Study:

To investigate whether the pathogenesis of adult HSPN is related to the imbalance of Th17/Treg cell axis.

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.研究组(过敏性紫癜性肾炎受试者)排除标准:
1) 妊娠期或哺乳期妇女;
2) 正在参与干预性临床实验;
3) 既往3个月内或正在因HSPN接受皮质激素及免疫抑制剂治疗者;
4)Ⅰ型或Ⅱ型糖尿病;
5) NYHA III级或IV级心力衰竭,即有基础心脏疾病,体力活动明显受限,小于一般体力活动甚至休息状态下即可出现疲乏、心悸、气喘或心绞痛症状;
6) 病毒性肝炎或肝硬化;
7) HIV感染或艾滋病;
8) 恶性肿瘤;
9) 既往接受超过1个月的透析治疗,和/或器官或骨髓移植;
10) 既往诊断为多囊肾等遗传性肾脏疾病。

2.对照组(健康受试者)排除标准:
1) 有高血压、糖尿病、冠心病、高尿酸血症或高脂血症等慢性病病史的人;
2) 有遗传病病史的人。
3)患有免疫性、过敏性疾病的患者;
4)恶性肿瘤患者。

Exclusion criteria:

1.Exclusion criteria of study group(HSPN subjects) :
1) Women during pregnancy or lactation;
2) Participating in interventional clinical trials
3) Patients who have been treated with glucocorticoids and immunosuppressants for the past 3 months or are being treated due to HSPN;
4) I or II type diabetes;
5) NYHA Class III or IV heart failure;
6) Viral hepatitis or cirrhosis;
7) HIV infection or AIDS;
8) Malignant tumors;
9) Have been receiving dialysis for more than 1month, and/or organ or bone marrow transplantation;
10) Have been diagnosed as polycystic kidney and other hereditary kidney diseases.

2.Exclusion criteria of control group(healthy subjects) :
1) Persons who have a history of chronic diseases such as hypertension, diabetes, coronary heart disease, hyperuricemia or hyperlipidemia;
2) Persons who have a history of genetic diseases;
3) Patients with immunological and allergic diseases;
4) Patients with malignant tumors.

研究实施时间:

Study execute time:

From 2019-08-01 00:00:00 To 2020-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2019-08-01 00:00:00 To 2019-12-31 00:00:00

干预措施:

Interventions:

组别:

紫癜性肾炎患者

样本量:

10

Group:

HSPN patients group

Sample size:

干预措施:

干预措施代码:

Intervention:

N/A

Intervention code:

组别:

健康对照组

样本量:

10

Group:

Healthy control group

Sample size:

干预措施:

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):

湖北省 

市(区县):

武汉 

Country:

China

Province:

Hubei

City:

Wuhan

单位(医院):

湖北省中医院 

单位级别:

三甲医院 

Institution
hospital:

Hubei Provincial Hospital of TCM

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

辅助性T细胞17,调节性T细胞

指标类型:

主要指标

Outcome:

Th17, Treg

Type:

Primary indicator

测量时间点:

测量方法:

流式细胞仪检测

Measure time point of outcome:

Measure method:

指标中文名:

白介素17,白介素10

指标类型:

主要指标

Outcome:

IL-17, IL-10

Type:

Primary indicator

测量时间点:

测量方法:

ELISA

Measure time point of outcome:

Measure method:

指标中文名:

维甲酸受体相关孤儿受体γt和叉头翼状螺旋核转录因子3

指标类型:

主要指标

Outcome:

RORγt, Foxp3

Type:

Primary indicator

测量时间点:

测量方法:

RT-PCR

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:

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 60 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):

不采用随机方法

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

Not used

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:

N/A

Blinding:

N/A

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):

2021年年初实验完成后公开,通过上传EXCELL文件至ResMan, http://www.medresman.org。

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

After the experiment is completed, it is disclosed by uploading the EXCELL file to ResMan, http://www.medresman.org.

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:

原始数据将由ResMan保管

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

Original data will be reposed by ResMan

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2019-08-14 22:49:05