Today is 2023-03-24

Prognosis evaluation of antiviral therapy for patients with chronic hepatitis B in immune tolerance stage
download

注册号:

Registration number:

ChiCTR2300067999 

最近更新日期:

Date of Last Refreshed on:

2023-02-02 

注册时间:

Date of Registration:

2023-02-02 

注册号状态:

补注册  

Registration Status:

Retrospective registration  

注册题目:

免疫耐受期慢乙肝患者抗病毒治疗预后评估方案  

Public title:

Prognosis evaluation of antiviral therapy for patients with chronic hepatitis B in immune tolerance stage 

注册题目简写:

 

English Acronym:

 

研究课题的正式科学名称:

免疫耐受期慢乙肝患者抗病毒治疗预后评估方案  

Scientific title:

Prognosis evaluation of antiviral therapy for patients with chronic hepatitis B in immune tolerance stage 

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:

张欢 

研究负责人:

雷学忠 

Applicant:

Huan Zhang 

Study leader:

XueZhong Lei 

申请注册联系人电话:

Applicant telephone:

13755208515 

研究负责人电话:

Study leader's telephone:

18980601317 

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:

1215398916@qq.com 

研究负责人电子邮件:

Study leader's E-mail:

18980601317@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:

四川省成都市武侯区国学巷37号 

研究负责人通讯地址:

四川省成都市武侯区国学巷37号 

Applicant address:

#37 Guoxue Alley, Wuhou District, Chengdu, Sichuan Province, China  

Study leader's address:

#37 Guoxue Alley, Wuhou District, Chengdu, Sichuan Province, China  

申请注册联系人邮政编码:

Applicant postcode:

610041 

研究负责人邮政编码:

Study leader's postcode:

610041 

申请人所在单位:

四川大学华西医院 

Applicant's institution:

West China Hospital of Sichuan University  

是否获伦理委员会批准:

是 

Approved by ethic committee:

Yes 

伦理委员会批件文号:

Approved No. of ethic committee:

2022年审(1126)号 

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:

四川大学华西医院生物医学伦理审查委员会 

Name of the ethic committee:

The Biomedical Ethics Review Committee of West China Hospital, Sichuan University  

伦理委员会批准日期:

Date of approved by ethic committee:

2022-07-15 

伦理委员会联系人:

彭淑贤 

Contact Name of the ethic committee:

ShuXian Peng 

伦理委员会联系地址:

四川省成都市武侯区国学巷37号 

Contact Address of the ethic committee:

#37 Guoxue Alley, Wuhou District, Chengdu, Sichuan Province, 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:

四川大学华西医院 

Primary sponsor:

West China Hospital, Sichuan University 

研究实施负责(组长)单位地址:

四川省成都市武侯区国学巷37号 

Primary sponsor's address:

#37 Guoxue Alley, Wuhou District, Chengdu, Sichuan Province, 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):

四川省

市(区县):

成都市

Country:

China

Province:

Sichuan province

City:

Chengdu city

单位(医院):

四川大学华西医院

具体地址:

武侯区国学巷37号

Institution
hospital:

West China Hospital of Sichuan University

Address:

#37 Guoxue Alley, Wuhou District

经费或物资来源:

无 

Source(s) of funding:

None 

研究疾病:

乙肝 

Target disease:

hepatitis B 

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:

其它 

Study phase:

N/A 

研究目的:

本研究旨在研究免疫耐受期慢乙肝患者的抗病毒治疗效果,评估GP73在治疗预后中的指导意义。 

Objectives of Study:

The purpose of this study was to investigate the efficacy of antiviral therapy in patients with chronic hepatitis B in immune-tolerant stage, and to evaluate the guiding significance of GP73 in treatment prognosis. 

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

研究设计:

队列研究 

Study design:

Cohort study 

纳入标准:

1、HBV DNA≥ 1.00E+07 IU/ML; 2、血清HBsAg阳性至少6个月以上,且HBeAg阳性; 3、血清ALT正常或<2x ULN; 4、近3个月内Fibroscan<9.0 Kpa和肝脏彩超提示无肝硬化,或近1年内肝脏组织病理学检查无明显炎症坏死或纤维化; 5、初治或经治患者均可。 

Inclusion criteria

1. HBV DNA≥ 1.00E+07 IU/ML; 2. Serum HBsAg positive for at least 6 months and HBeAg positive; 3. Serum ALT was normal or < 2x ULN; 4. No liver cirrhosis was indicated by Fibroscan < 9.0kpa and liver color ultrasound within the last 3 months, or no obvious inflammatory necrosis or fibrosis was observed by liver histopathological examination within the last 1 year; 5. All patients can be treated initially or after treatment. 

排除标准:

1、合并肝硬化、肿瘤、结缔组织病等; 2、排除酒精肝、药物性肝炎、自身免疫性肝炎、甲丙戊肝炎等; 3、存在心、肺、肝、肾等其他系统严重功能障碍; 4、患有严重的精神疾病,怀孕、哺乳期受试者; 5、其他研究者认为不适合参加研究的情况。 

Exclusion criteria:

1. Cirrhosis, tumor, connective tissue disease, etc.; 2. Exclude alcoholic liver, drug hepatitis, autoimmune hepatitis, hepatitis A vale, etc.; 3. Serious dysfunction of heart, lung, liver, kidney and other systems; 4. Subjects with serious mental illness, pregnancy or lactation; 5. Conditions that other researchers consider unsuitable for participating in the study. 

研究实施时间:

Study execute time:

From2022-08-01To 2024-12-31 

征募观察对象时间:

Recruiting time:

From2022-08-01To 2024-12-31 

干预措施:

Interventions:

组别:

免疫耐受期抗病毒组

样本量:

80

Group:

Immune tolerance period antiviral group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

组别:

免疫耐受期未抗病毒组

样本量:

20

Group:

Immune tolerance period without antiviral group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

组别:

GP73正常组

样本量:

80

Group:

GP73 normal group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

组别:

GP73异常组

样本量:

80

Group:

Abnormal GP73 group

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):

四川省 

市(区县):

成都市 

Country:

China 

Province:

Sichuan province 

City:

Chengdu city 

单位(医院):

四川大学华西医院 

单位级别:

三级甲等 

Institution
hospital:

West China Hospital of Sichuan University  

Level of the institution:

Grade 3A hospital 

测量指标:

Outcomes:

指标中文名:

HBVDNA定量

指标类型:

主要指标 

Outcome:

HBVDNA quantification

Type:

Primary indicator 

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

GP73

指标类型:

次要指标 

Outcome:

GP73

Type:

Secondary indicator 

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

HBsAg定量

指标类型:

次要指标 

Outcome:

HBsAg quantification

Type:

Secondary indicator 

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

HBeAg定量

指标类型:

次要指标 

Outcome:

HBeAg quantification

Type:

Secondary indicator 

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

ALT定量

指标类型:

次要指标 

Outcome:

ALT quantification

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:

组织:

Sample Name:

No

Tissue:

人体标本去向

其它 

说明

Fate of sample:

Others 

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 15 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):

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

None

盲法:

Blinding:

试验完成后的统计结果(上传文件):

Calculated Results ater
the Study Completed(upload file):

是否共享原始数据:

IPD sharing

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):

临床试验公共管理平台(http://www.medresman.org.cn)。

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

ResMan (http://www.medresman.org.cn)

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/电子病例记录表

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

CRF/EDC

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2023-02-02
return list