ChiCTR2100048427 版本V1.2 版本创建时间2022/03/14 12:32:42 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:

ChiCTR2100048427 

最近更新日期:

Date of Last Refreshed on:

2021-07-06 18:48:42 

注册时间:

Date of Registration:

2021-07-06 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

前列腺癌诊断及预后模型多中心研究

Public title:

Multicenter study of prostate cancer diagnosis and prognosis model

注册题目简写:

English Acronym:

研究课题的正式科学名称:

前列腺癌诊断及预后模型多中心研究

Scientific title:

Multicenter study of prostate cancer diagnosis and prognosis model

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:

陈锐 

研究负责人:

陈锐 

Applicant:

Chen Rui 

Study leader:

Chen Rui 

申请注册联系人电话:

Applicant telephone:

+86 13764301103

研究负责人电话:

Study leader's
telephone:

+86 13764301103

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:

drchenrui@foxmail.com

研究负责人电子邮件:

Study leader's E-mail:

drchenrui@foxmail.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:

上海市长海路168号

研究负责人通讯地址:

上海市长海路168号

Applicant address:

168 Changhai Road, Yangpu District, Shanghai, China

Study leader's address:

168 Changhai Road, Yangpu District, Shanghai, 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:

海军军医大学第一附属医院

Applicant's institution:

The First Affiliated Hospital of Naval Medical University

研究负责人所在单位:

海军军医大学第一附属医院

Affiliation of the Leader:

The First Affiliated Hospital of Naval Medical University

是否获伦理委员会批准:

Approved by ethic committee:

No

伦理委员会批件文号:

Approved No. of ethic committee:

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:

Name of the ethic committee:

伦理委员会批准日期:

Date of approved by ethic committee:

2013-08-26 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:

海军军医大学第一附属医院

Primary sponsor:

The First Affiliated Hospital of Naval Medical University

研究实施负责(组长)单位地址:

上海市长海路168号

Primary sponsor's address:

168 Changhai Road, Yangpu District, Shanghai, 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):

上海

市(区县):

Country:

China

Province:

Shanghai

City:

单位(医院):

海军军医大学第一附属医院

具体地址:

上海市长海路168号

Institution
hospital:

The First Affiliated Hospital of Naval Medical University

Address:

168 Changhai Road

经费或物资来源:

自主筹集

Source(s) of funding:

Self-raising

研究疾病:

前列腺癌  

Target disease:

Prostate cancer

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:

回顾性研究 

Study phase:

Retrospective study

研究设计:

连续入组 

Study design:

Sequential 

研究目的:

旨在开发和验证一种风险计算器,用于预测中国男性初次前列腺活检时发生PCa和HGPCa(Gleason 评分总和≥ 7)的概率。  

Objectives of Study:

aimed to develop and validate a risk calculator for predicting the probability of PCa and high-grade PCa (defined as Gleason Score sum 7 or higher) at initial prostate biopsy in Chinese men.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

- 年龄>40岁
- PSA ≥ 4.0 ng/ml、直肠指检 (DRE) 异常或经直肠超声 (TRUS) 成像有可疑病变

Inclusion criteria

- Aged 40 to 90 years;
- PSA levels greater than 4.0 ng/ml or abnormal DRE or those who have suspicious imaging findings.

排除标准:

- PSA 大于 50 ng/ml 的患者(根据 ERSPC-RC)
- 游离PSA比率大于0.5(排除极端值)
- PV 大于 150 毫升(符合 ERSPC-RC);
- 年龄小于 40 岁或大于 90 岁;
- 重复活检
- 过去 2 周内有尿路感染、尿潴留和尿道器械或导尿的患者,患者在过去 2 个月内接受过 5α-还原酶抑制剂

Exclusion criteria:

- patients with PSA greater than 50 ng/ml (in accordance with ERSPC-RC);
- free PSA ratio greater than 0.5 (to exclude extreme values);
- PV greater than 150 ml (in accordance with ERSPC-RC);
- repeat biopsies;
- patients with urinary tract infections, urinary retention, and instrumentation or catheterization of the urethra within the past 2 weeks,patients received 5α-reductase inhibitors within the last 2 months.

研究实施时间:

Study execute time:

From 2011-01-01 00:00:00 To 2013-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2011-01-01 00:00:00 To 2013-12-31 00:00:00

干预措施:

Interventions:

组别:

Case series

样本量:

2508

Group:

Case series

Sample size:

干预措施:

Nil

干预措施代码:

Intervention:

Nil

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

上海 

市(区县):

 

Country:

China

Province:

Shanghai

City:

单位(医院):

海军军医大学第一附属医院 

单位级别:

三级甲等医院 

Institution
hospital:

The First Affiliated Hospital of Naval Medical University

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

浙江 

市(区县):

 

Country:

China

Province:

Zhejiang

City:

单位(医院):

浙江大学第一附属医院 

单位级别:

三级甲等医院 

Institution
hospital:

The First Affiliated Hospital of Zhejiang University

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

上海 

市(区县):

 

Country:

China

Province:

Shanghai

City:

单位(医院):

上海交通大学瑞金医院 

单位级别:

三级甲等医院 

Institution
hospital:

Renji Hospital of Shanghai Jiao Tong University

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

湖北 

市(区县):

武汉 

Country:

China

Province:

Hubei

City:

Wuhan

单位(医院):

华中科技大学同济医院 

单位级别:

三级甲等医院 

Institution
hospital:

Tongji Hospital of Huazhong University of Science and Technology

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

北京 

市(区县):

 

Country:

China

Province:

Beijing

City:

单位(医院):

北京大学第三医院 

单位级别:

三级甲等医院 

Institution
hospital:

Peking University Third Hospital

Level of the institution:

Tertiary A Hospital

国家:

荷兰

省(直辖市):

鹿特丹 

市(区县):

 

Country:

Netherlands

Province:

Rotterdam

City:

单位(医院):

鹿特丹伊拉斯姆斯大学医学中心 

单位级别:

三级甲等医院 

Institution
hospital:

Erasmus Universuty Medical Center

Level of the institution:

Tertiary A Hospital

测量指标:

Outcomes:

指标中文名:

前列腺特异性抗原

指标类型:

主要指标

Outcome:

PSA

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:

征募研究对象情况:

Recruiting status:

结束

/Completed

年龄范围:

Participant age:

最小 Min age 63 years
最大 Max age 75 years

性别:

男性

Gender:

Male

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

是否公开试验完成后的统计结果:

Calculated Results after the Study Completed public access:

不公开/Private

盲法:

N/A

Blinding:

N/A

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):

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

None

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:

数据收集利用病例报告表来完成。

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

Data collection is mainly collected through thepathology report form.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2021-07-06 18:44:10