ChiCTR2300077354 版本V1.0 版本创建时间2023/11/06 16:20:50 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2300077354 

最近更新日期:

Date of Last Refreshed on:

2023-11-06 16:19:20 

注册时间:

Date of Registration:

2023-11-06 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

急性白血病复发预测生物学标记物研发及临床转化——多指标联合检测预测急性白血病复发的前瞻性队列研究

Public title:

Development and Clinical Transformation of Biological Markers for Predicting Acute Leukemia Relapse: A Prospective Cohort Study of Multiple Indicators for Predicting Acute Leukemia Relapse

注册题目简写:

English Acronym:

研究课题的正式科学名称:

急性白血病复发预测生物学标记物研发及临床转化——多指标联合检测预测急性白血病复发的前瞻性队列研究

Scientific title:

Development and Clinical Transformation of Biological Markers for Predicting Acute Leukemia Relapse: A Prospective Cohort Study of Multiple Indicators for Predicting Acute Leukemia Relapse

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:

常英军 

研究负责人:

常英军 

Applicant:

Chang Yingjun  

Study leader:

Chang Yingjun  

申请注册联系人电话:

Applicant telephone:

+86 10 8832 5949

研究负责人电话:

Study leader's
telephone:

+86 10 8832 5949

申请注册联系人传真 :

Applicant Fax:

研究负责人传真:

Study leader's fax:

010-88324577

申请注册联系人电子邮件:

Applicant E-mail:

rmcyj@bjmu.edu.cn

研究负责人电子邮件:

Study leader's E-mail:

rmcyj@bjmu.edu.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:

北京大学人民医院科研楼518室;北京市西城区西直门南大街11号

研究负责人通讯地址:

北京大学人民医院科研楼518室;北京市西城区西直门南大街11号

Applicant address:

11 South Street of Xizhimen, Xicheng District, Beijing, China

Study leader's address:

11 South Street of Xizhimen, Xicheng District, Beijing, 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:

北京大学人民医院/北京大学血液病研究所

Applicant's institution:

Peking University People's Hospital & Peking University Institute of Hematology

研究负责人所在单位:

北京大学人民医院/北京大学血液病研究所

Affiliation of the Leader:

Peking University People's Hospital & Peking University Institute of Hematology

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:

2023PHB164-001

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:

北京大学人民医院伦理审查委员会

Name of the ethic committee:

Ethics Committee of Peking University People's Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2023-05-23 00:00:00

伦理委员会联系人:

母双

Contact Name of the ethic committee:

Mu Shuang

伦理委员会联系地址:

北京市西城区西直门南大街11号

Contact Address of the ethic committee:

11 South Street of Xizhimen, Xicheng District, Beijing, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 10 8832 4516

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:

北京大学人民医院/北京大学血液病研究所

Primary sponsor:

Peking University People's Hospital & Peking University Institute of Hematology

研究实施负责(组长)单位地址:

北京市西城区西直门南大街11号

Primary sponsor's address:

11 South Street of Xizhimen, Xicheng District, Beijing, 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):

北京

市(区县):

Country:

China

Province:

Beijing

City:

单位(医院):

北京大学人民医院

具体地址:

西城区西直门南大街11号

Institution
hospital:

Peking University People's Hospital

Address:

11 South Street of Xizhimen, Xicheng District

经费或物资来源:

北京市科技计划项目

Source(s) of funding:

Beijing Municipal Science and Technology Project

研究疾病:

急性白血病  

Target disease:

Acute Leukemia

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:

探索性研究/预试验 

Study phase:

0

研究设计:

连续入组 

Study design:

Sequential 

研究目的:

探究及确立一种更加有效的预测AL患者复发的检测手段  

Objectives of Study:

Exploring and establishing a more effective detection method for predicting relapse in AL 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:

1.初诊急性白血病(AL)患者; 2.年龄18~60岁。

Inclusion criteria

1.Patients with newly diagnosed acute leukemia; 2.Aged 18 to 60 years.

排除标准:

1.不能接受诱导化疗者; 2.患者缺乏依从性。

Exclusion criteria:

1.Subjects who cannot receive induction chemotherapy; 2.Subjects who cannot comply with the study.

研究实施时间:

Study execute time:

From 2023-11-10 00:00:00 To 2026-11-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2023-11-10 00:00:00 To 2026-11-01 00:00:00

干预措施:

Interventions:

组别:

Case series

样本量:

360

Group:

Case series

Sample size:

干预措施:

干预措施代码:

Intervention:

NA

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

北京 

市(区县):

 

Country:

China

Province:

Beijing

City:

单位(医院):

北京大学人民医院 

单位级别:

三级甲等  

Institution
hospital:

Peking University People's Hospital

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

北京 

市(区县):

 

Country:

China

Province:

Beijing

City:

单位(医院):

北京大学第一医院 

单位级别:

三级甲等  

Institution
hospital:

Peking University First Hospital

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

北京 

市(区县):

 

Country:

China

Province:

Beijing

City:

单位(医院):

中国人民解放军总医院第五医学中心 

单位级别:

三级甲等  

Institution
hospital:

The Fifth Medical Center of the General Hospital of the People's Liberation Army of China

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

复发率

指标类型:

主要指标

Outcome:

Relapse rate

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

无病生存

指标类型:

次要指标

Outcome:

Leukemia-free survival

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

总体生存

指标类型:

次要指标

Outcome:

Overall survival

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

非复发死亡/移植相关死亡

指标类型:

次要指标

Outcome:

Non-relapse mortality/Transplantation-related mortality

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

急性/慢性移植物抗宿主病

指标类型:

次要指标

Outcome:

Acute/ chronic graft-versus-host disease

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:

骨髓

组织:

外周血

Sample Name:

Bone marrow

Tissue:

Peripheral blood

人体标本去向

使用后保存  

说明

Fate of sample:

Preservation after use  

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 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):

非随机对照试验

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

Non randomized controlled trial

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:

None

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

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):

北京大学人民医院临床数据中心 http://10.8.4.43:8001/cdr/login.html

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

Clinical Data Center, Peking University People's Hospital, http://10.8.4.43:8001/cdr/login.html

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:

电子采集和管理系统

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

Electronic Data Capture, EDC

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2023-11-06 16:19:20