聚乙二醇干扰素α-2a个体化治疗慢性乙肝患者的临床疗效及其与肝组织Knodell HAI评分的关系

注册号:

Registration number:

ChiCTR-OCC-12002196 

最近更新日期:

Date of Last Refreshed on:

2015-08-13 21:27:36 

注册时间:

Date of Registration:

2012-05-24 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

聚乙二醇干扰素α-2a个体化治疗慢性乙肝患者的临床疗效及其与肝组织Knodell HAI评分的关系

Public title:

The Efficacy of Individualized PEG-IFNalpha-2a Therapy in Patients with Chronic Hepatitis B and the Association between Efficacy and Hepatic Histology

注册题目简写:

English Acronym:

研究课题的正式科学名称:

聚乙二醇干扰素α-2a个体化治疗慢性乙肝患者的临床疗效及其与肝组织Knodell HAI评分的关系

Scientific title:

The Efficacy of Individualized PEG-IFNalpha-2a Therapy in Patients with Chronic Hepatitis B and the Association between Efficacy and Hepatic Histology

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:

徐严 

研究负责人:

王江滨 

Applicant:

Xu Yan 

Study leader:

Wang Jiangbin 

申请注册联系人电话:

Applicant telephone:

+86 13514481674

研究负责人电话:

Study leader's
telephone:

+86 0431 84995303

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:

zrlxuyan@163.com

研究负责人电子邮件:

Study leader's E-mail:

zrlwangjb@medmail.com.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:

吉林省长春市仙台大街126号

研究负责人通讯地址:

吉林省长春市仙台大街126号

Applicant address:

126 Xiantai BLVD, Changchun, Jilin, China

Study leader's address:

126 Xiantai BLVD, Changchun, Jilin, China

申请注册联系人邮政编码:

Applicant postcode:

130033

研究负责人邮政编码:

Study leader's postcode:

130033

申请人所在单位:

吉林大学中日联谊医院

Applicant's institution:

China-Japan union hospital of Jilin university

研究负责人所在单位:

Affiliation of the Leader:

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:

20111110

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:

吉林大学中日联谊医院伦理委员会

Name of the ethic committee:

China-Japan union hospital of Jilin university Ethics Committee

伦理委员会批准日期:

Date of approved by ethic committee:

2011-01-11 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:

吉林大学中日联谊医院

Primary sponsor:

China-Japan union hospital of Jilin university

研究实施负责(组长)单位地址:

吉林省长春市仙台大街126号

Primary sponsor's address:

126 Xiantai BLVD, Changchun, Jilin, 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):

吉林

市(区县):

长春

Country:

China

Province:

Jilin

City:

Changchun

单位(医院):

吉林大学中日联谊医院

具体地址:

吉林省长春市仙台大街126号

Institution
hospital:

126 XIANTAI BLVD, Changchun,Jilin province

Address:

126 Xiantai BLVD, Changchun, Jilin, China

经费或物资来源:

吉林省科技厅项目

Source(s) of funding:

Science and Technology Department of Jilin Province Project

研究疾病:

慢性乙肝  

Target disease:

chronic 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:

上市后药物 

Study phase:

4

研究设计:

病例对照研究 

Study design:

Case-Control study 

研究目的:

对长期应用聚乙二醇干扰素α-2a(Peg-INFα-2a)治疗的慢性乙肝患者的临床特征进行分析,探讨延长疗程和联合核苷(酸)类似物治疗对应答率及持久应答的影响,并评价了其对肝组织学改善状况,为个体化治疗慢性乙肝提供进一步的循证医学依据。  

Objectives of Study:

To investigate the efficacy of individualized therapy with PEG-IFNalpha-2a and the effect of antiviral therapy on hepatic histology in chronic hepatitis B 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:

Inclusion criteria

排除标准:

1、妊娠期及哺乳期;2、除外失代偿期肝硬化;3、无精神病史、癫痫、恶性肿瘤、有症状的心脏病;4、无吸毒或酗酒史,未合并HCV、HDV及HIV感染等。

Exclusion criteria:

The exclusion criteria were: pregnancy or lactation; decompensated cirrhosis; history of psychiatric disorders, epilepsy, malignancies, or symptomatic heart diseases; history of drug or alcohol abuse; and co-infection with HCV, HDV, and HIV.

研究实施时间:

Study execute time:

From 2005-09-01 00:00:00 To 2010-03-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2005-09-01 00:00:00 To 2010-03-01 00:00:00

干预措施:

Interventions:

组别:

1

样本量:

40

Group:

one

Sample size:

干预措施:

延长疗程至72周

干预措施代码:

Intervention:

prolonged treatment group received 72 weeks of treatment

Intervention code:

组别:

2

样本量:

39

Group:

two

Sample size:

干预措施:

联合恩替卡韦组

干预措施代码:

Intervention:

combination with entecavir

Intervention code:

组别:

3

样本量:

36

Group:

three

Sample size:

干预措施:

联合阿德福韦酯组

干预措施代码:

Intervention:

combination with adefovir dipivoxil

Intervention code:

组别:

4

样本量:

33

Group:

four

Sample size:

干预措施:

常规48周疗程

干预措施代码:

Intervention:

combination with adefovir dipivoxil

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

吉林 

市(区县):

长春 

Country:

China

Province:

Jilin

City:

Changchun

单位(医院):

吉林大学中日联谊医院 

单位级别:

三级甲等医院 

Institution
hospital:

China-Japan union hospital of Jilin university

Level of the institution:

Tertiary A hospital

测量指标:

Outcomes:

指标中文名:

HBV DNA

指标类型:

主要指标

Outcome:

HBV DNA

Type:

Primary 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:

主要指标

Outcome:

quantitative HBsAg

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

肝功能

指标类型:

次要指标

Outcome:

liver function

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

HBV血清学标志

指标类型:

次要指标

Outcome:

serum HBV biomarkers

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

肝组织学评分

指标类型:

次要指标

Outcome:

Knodell HAI

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:

血液

组织:

肝脏

Sample Name:

blood

Tissue:

liver

人体标本去向

使用后销毁  

说明

肝组织病理科保存

Fate of sample:

Destruction after use  

Note:

Department of Pathology, preservation

征募研究对象情况:

Recruiting status:

结束

/Completed

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 65 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):

本研究根据12周HBV DNA定量检测结果,对未达到早期病毒学应答的患者进行分组比较,是在与患者沟通、知情同意的情况下进行分组比较。

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

The regimen was individualized according to the response at 12 weeks of antiviral therapy,and commun

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:

Blinding:

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

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):

吉林大学中日联谊医院

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

China-Japan union hospital of Jilin university

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:

吉林大学中日联谊医院

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

China-Japan union hospital of Jilin university

数据与安全监察委员会:

Data and Safety Monitoring Committee:

注册人:

Name of Registration:

 2012-05-28 00:00:00