ChiCTR2200066614 版本V1.2 版本创建时间2023/08/20 22:20:12 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:

ChiCTR2200066614 

最近更新日期:

Date of Last Refreshed on:

2023-05-07 23:10:41 

注册时间:

Date of Registration:

2022-12-12 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

肿瘤治疗相关血小板减少症全国多中心真实世界研究

Public title:

A Multicenter Real-world Study of Cancer Therapy Induced Thrombocytopenia(CTIT) in China

注册题目简写:

English Acronym:

研究课题的正式科学名称:

肿瘤治疗相关血小板减少症全国多中心真实世界研究

Scientific title:

A Multicenter Real-world Study of Cancer Therapy Induced Thrombocytopenia(CTIT) in China

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:

赵东陆 

研究负责人:

马军/秦叔逵 

Applicant:

Donglu Zhao 

Study leader:

Jun Ma/Shukui Qin 

申请注册联系人电话:

Applicant telephone:

+86 13936254716

研究负责人电话:

Study leader's
telephone:

+86 13304518000

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:

huu7kx@163.com

研究负责人电子邮件:

Study leader's E-mail:

majun0322@126.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:

哈尔滨市道里区地段街149号

研究负责人通讯地址:

哈尔滨市道里区地段街149号

Applicant address:

149 Diduan Street Daoli District, Harbin

Study leader's address:

149 Diduan Street Daoli District, Harbin

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:

哈尔滨血液病肿瘤研究所

Applicant's institution:

Harbin Institute of Hematology and Oncology

研究负责人所在单位:

哈尔滨血液病肿瘤研究所

Affiliation of the Leader:

Harbin Institute of Hematology and Oncology

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:

临伦审第( 2022-003)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:

哈尔滨市第一医院血液肿瘤研究中心伦理委员会

Name of the ethic committee:

Harbin Institute of Hematology and Oncology Ethical Committee

伦理委员会批准日期:

Date of approved by ethic committee:

2022-04-08 00:00:00

伦理委员会联系人:

程梅

Contact Name of the ethic committee:

Mei Cheng

伦理委员会联系地址:

哈尔滨市道里区地段街149号

Contact Address of the ethic committee:

149 Diduan Street Daoli District, Harbin

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 451 84883432

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:

哈尔滨血液病肿瘤研究所

Primary sponsor:

Harbin Institute of Hematology and Oncology

研究实施负责(组长)单位地址:

哈尔滨市道里区地段街149号

Primary sponsor's address:

149 Diduan Street Daoli District, Harbin

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

黑龙江

市(区县):

哈尔滨

Country:

China

Province:

Heilongjiang

City:

Harbin

单位(医院):

哈尔滨血液病肿瘤研究所

具体地址:

哈尔滨市道里区地段街149号

Institution
hospital:

Harbin Institute of Hematology and Oncology

Address:

149 Diduan Street Daoli District, Harbin

经费或物资来源:

江苏恒瑞医药股份有限公司

Source(s) of funding:

Jiangsu Hengrui Pharmaceuticals Co., Ltd

研究疾病:

肿瘤治疗相关血小板减少症  

Target disease:

Cancer Therapy Induced Thrombocytopenia

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:

队列研究 

Study design:

Cohort study 

研究目的:

探索中国肿瘤治疗相关血小板减少症的疾病特征和治疗模式  

Objectives of Study:

Explore the disease feature and treatment pattern of Cancer Therapy Induced Thrombocytopenia in China

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.理解研究程序且自愿签署知情同意书,自愿加入本研究;
2.年龄≥18岁,接受抗肿瘤治疗(包括化疗、放疗、靶向治疗、免疫治疗等);
3.血小板计数≤100×10*9/L或血小板计数下降≥ 50×10*9/L或血小板计数> 100×10*9/L但需要进行CIT预防的患者;
4.研究者认为需要接受促血小板生成药物:rhTPO, rhIL-11, TPO-RA(艾曲泊帕,海曲泊帕,阿伐曲泊帕)类药物治疗;

Inclusion criteria

1.Signed ICF for voluntary participation in the study and good compliance
2.age ≥18 years,receiving a Cancer Therapy(including chemotherapy,radiotherapy, targeted therapy or immunotherapy
3.PLT≤100×10*9/L or PLT> 100×10*9/L but need the prevention of CIT
4.Administration of hematopoietic growth factor(including rhTPO,rhIL-11 and TPO-RA)

排除标准:

1.患者正在进行临床干预性研究;
2.无法理解研究的研究性质或未获得知情同意;
3.研究者判断其他不适合纳入研究的情况。

Exclusion criteria:

1.Participation in another interventional clinical trial
2.Unable to understand the investigational nature of the study or give informed consent
3.Investigator's judgement that participation not suitable for the study

研究实施时间:

Study execute time:

From 2022-09-01 00:00:00 To 2024-09-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-12-20 00:00:00 To 2024-09-01 00:00:00

干预措施:

Interventions:

组别:

肿瘤治疗相关血小板减少症组

样本量:

3000

Group:

Group of cancer Therapy Induced Thrombocytopenia

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):

黑龙江 

市(区县):

 

Country:

China

Province:

Heilongjiang

City:

单位(医院):

哈尔滨血液病肿瘤研究所 

单位级别:

Institution
hospital:

Harbin Institute of Hematology and Oncology

Level of the institution:

1

国家:

中国

省(直辖市):

黑龙江省 

市(区县):

 

Country:

China

Province:

heilongjiang

City:

单位(医院):

佳木斯大学附属第一医院 

单位级别:

Institution
hospital:

THE FIRST AFFILIATED HOSPITAL OF JIAMUSI UNIVERSITY

Level of the institution:

1

测量指标:

Outcomes:

指标中文名:

肿瘤治疗相关血小板减少症的疾病特征和治疗模式

指标类型:

主要指标

Outcome:

the disease feature and treatment pattern of Cancer Therapy Induced Thrombocytopenia

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

安全性

指标类型:

次要指标

Outcome:

safety

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

有效性

指标类型:

次要指标

Outcome:

Effectiveness

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:

不适用

组织:

Sample Name:

Not Applicable

Tissue:

人体标本去向

其它  

说明

不适用

Fate of sample:

0thers  

Note:

Not Applicable

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 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):

不适用

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

Not applicable

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:

不适用

Blinding:

Not applicable

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):

不适用

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

Not applicable

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:

1.病例记录表; 2.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:

CRF;EDC

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2022-12-12 11:58:30