中国艾滋病感染者更换二线抗病毒治疗方案后的疗效观察

注册号:

Registration number:

ChiCTR-OCH-14004522 

最近更新日期:

Date of Last Refreshed on:

2016-09-17 16:54:59 

注册时间:

Date of Registration:

2014-04-09 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

中国艾滋病感染者更换二线抗病毒治疗方案后的疗效观察

Public title:

Treatment effect and drug-resistant mutations in Chinese AIDS patients switching to second-line antiretroviral therapy

注册题目简写:

English Acronym:

研究课题的正式科学名称:

中国艾滋病感染者更换二线抗病毒治疗方案后的疗效观察

Scientific title:

surveillance and testing technology of HIV resistant strains and its clinical application in China

研究课题代号(代码):

Study subject ID:

十二五国家科技重大专项项目 (2012ZX10001002-002-013)

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:

陈俊丽 

研究负责人:

张旻 

Applicant:

Junli Chen 

Study leader:

Min Zhang 

申请注册联系人电话:

Applicant telephone:

+86 13840157117

研究负责人电话:

Study leader's
telephone:

+86 18040095420

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:

cmucjl@126.com

研究负责人电子邮件:

Study leader's E-mail:

minzhang_100@hotmail.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:

辽宁省沈阳市和平区南京北街155号中国医科大学附属第一医院艾滋病研究所

研究负责人通讯地址:

辽宁省沈阳市和平区南京北街155号中国医科大学附属第一医院艾滋病研究所

Applicant address:

155 North Nanjing Street, Shenyang, China

Study leader's address:

155 North Nanjing Street, Shenyang, Liaoning, China

申请注册联系人邮政编码:

Applicant postcode:

110001

研究负责人邮政编码:

Study leader's postcode:

110001

申请人所在单位:

中国医科大学附属第一医院

Applicant's institution:

The First Affiliated Hospital, China Medical University

研究负责人所在单位:

中国医科大学附属第一医院

Affiliation of the Leader:

The First Affiliated Hospital, China Medical University

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:

[2013]13

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:

中国医科大学附属第一医院医学科学研究伦理委员会

Name of the ethic committee:

the Institutional Review Board of the First Affiliated Hospital of China Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2013-02-19 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:

中国医科大学附属第一医院艾滋病研究所

Primary sponsor:

Key Laboratory of AIDS Immunology of National Health and Family Planning Commission, Department of Laboratory Medicine, The First Affiliated Hospital, China Medical University

研究实施负责(组长)单位地址:

辽宁省沈阳市和平区南京北街155号

Primary sponsor's address:

155 North Nanjing Street, Shenyang, Liaoning, 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):

河南

市(区县):

尉氏

Country:

China

Province:

Henan

City:

Weishi

单位(医院):

河南省疾病预防控制中心

具体地址:

Institution
hospital:

Disease Prevention and Control Center of Henan Province

Address:

经费或物资来源:

十二五国家科技重大专项项目 (2012ZX10001002-002-013)

Source(s) of funding:

the Twelfth Five-Year Project on Tackling Key Problems of National Science and Technology (2012ZX10001002-002-013)

研究疾病:

艾滋病  

Target disease:

AIDS

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

研究设计:

队列研究 

Study design:

Cohort study 

研究目的:

明确我国二线抗病毒治疗方案的治疗效果和HIV耐药性变化,以及影响二线抗病毒治疗效果的相关因素,从而为二线抗病毒治疗方案在中国扩大规模提供重要的信息依据。  

Objectives of Study:

Investigate treatment effect, drug resistance changes, and their influencing factors in Chinese AIDS patients after switching to second-line antiretroviral therapy, and thus provide important information for the scale-up of second-line antiretroviral treatment in China

药物成份或治疗方案详述:

替诺福韦(TDF)+克立芝(利托那韦与洛匹那韦合剂)+拉米夫定(3TC) 

Description for medicine or protocol of treatment in detail:

Tenofovir (TDF) + Kaletra (ritonavir and lopinavir mixture) + lamivudine (3TC) 

纳入标准:

Inclusion criteria

排除标准:

未接受过一线抗病毒治疗的新发感染者

Exclusion criteria:

HIV infected patients who did not receive first-line antiretroviral therapy.

研究实施时间:

Study execute time:

From 2009-08-01 00:00:00 To 2011-12-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2009-08-01 00:00:00 To 2010-02-01 00:00:00

干预措施:

Interventions:

组别:

符合二线换药标准

样本量:

127

Group:

patients who met the second-line treatment criteria

Sample size:

干预措施:

替诺福韦(TDF)+克立芝(利托那韦与洛匹那韦合剂)+拉米夫定(3TC)药物组合方案进行抗病毒治疗

干预措施代码:

Intervention:

Tenofovir (TDF) + Kaletra (ritonavir and lopinavir mixture) + lamivudine (3TC)combination antiretroviral therapy

Intervention code:

组别:

不符合二线换药标准

样本量:

68

Group:

patients who did not meet the second-line treatment

Sample size:

干预措施:

替诺福韦(TDF)+克立芝(利托那韦与洛匹那韦合剂)+拉米夫定(3TC)药物组合方案进行抗病毒治疗

干预措施代码:

Intervention:

Tenofovir (TDF) + Kaletra (ritonavir and lopinavir mixture) + lamivudine (3TC)combination antiretroviral therapy

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

湖南 

市(区县):

尉氏 

Country:

China

Province:

Henan

City:

Weishi

单位(医院):

河南省疾病预防控制中心 

单位级别:

省级 

Institution
hospital:

Disease Prevention and Control Center of Henan Province

Level of the institution:

provincial

测量指标:

Outcomes:

指标中文名:

CD4+ T细胞

指标类型:

主要指标

Outcome:

CD4+T lymphocyte

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

HIV病毒载量

指标类型:

主要指标

Outcome:

Viral load measurement

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

HIV耐药突变

指标类型:

主要指标

Outcome:

HIV Drug-resistant mutation

Type:

Primary 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:

外周静脉采血

Sample Name:

blood

Tissue:

Peripheral venous

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:

结束

/Completed

年龄范围:

Participant age:

最小 Min age 32 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):

非随机抽样

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

not a Randomization Procedure

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

否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):

中国医科大学附属第一医院

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

The First Affiliated Hospital, China Medical 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:

中国医科大学附属第一医院

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

The First Affiliated Hospital, China Medical University

数据与安全监察委员会:

Data and Safety Monitoring Committee:

注册人:

Name of Registration:

 2014-04-17 00:00:00