ChiCTR2400093612 版本V1.0 版本创建时间2024/12/09 15:20:39 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:

ChiCTR2400093612 

最近更新日期:

Date of Last Refreshed on:

2024-12-09 15:20:17 

注册时间:

Date of Registration:

2024-12-09 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

PSA灰色地带患者血清及尿液微生态研究

Public title:

Study on serum and urine microbiota in patients with PSA in the gray zone

注册题目简写:

English Acronym:

研究课题的正式科学名称:

PSA灰色地带患者血清及尿液微生态研究

Scientific title:

Study on serum and urine microbiota in patients with PSA in the gray zone

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:

沈扬 

研究负责人:

冯宁翰 

Applicant:

Yang Shen 

Study leader:

Ninghan Feng 

申请注册联系人电话:

Applicant telephone:

+86 181 9514 8459

研究负责人电话:

Study leader's
telephone:

+86 138 6189 2528

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:

youngshen@stu.njmu.edu.cn

研究负责人电子邮件:

Study leader's E-mail:

n.feng@njmu.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:

江苏省无锡市梁溪区崇安寺街道

研究负责人通讯地址:

江苏省无锡市梁溪区中山路68号

Applicant address:

Chongan Temple Street, Liangxi District, Wuxi City, Jiangsu Province

Study leader's address:

No.68 Zhongshan Road, Liangxi District, Wuxi City, Jiangsu Province

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:

南京医科大学

Applicant's institution:

Nanjing Medical University

研究负责人所在单位:

江南大学附属中心医院

Affiliation of the Leader:

Jiangnan University Medical Center

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:

(2023)伦理审查第(Y-168)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:

江南大学附属中心医院伦理委员会

Name of the ethic committee:

the Ethics Committee of Jiangnan University Medical Center

伦理委员会批准日期:

Date of approved by ethic committee:

2023-12-15 00:00:00

伦理委员会联系人:

夏加增

Contact Name of the ethic committee:

Jiazeng Xia

伦理委员会联系地址:

江苏省无锡市梁溪区中山路68号

Contact Address of the ethic committee:

No.68 Zhongshan Road, Liangxi District, Wuxi City, Jiangsu Province

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 139 2112 8288

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:

江南大学附属中心医院

Primary sponsor:

Jiangnan University Medical Center

研究实施负责(组长)单位地址:

江苏省无锡市梁溪区中山路68号

Primary sponsor's address:

No.68 Zhongshan Road, Liangxi District, Wuxi City, Jiangsu Province

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

江苏

市(区县):

Country:

China

Province:

Jiangsu

City:

单位(医院):

江南大学附属中心医院

具体地址:

江苏省无锡市梁溪区中山路68号

Institution
hospital:

Jiangnan University Medical Center

Address:

No.68 Zhongshan Road, Liangxi District, Wuxi City, Jiangsu Province

经费或物资来源:

中国国家自然科学基金

Source(s) of funding:

The National Natural Science Foundation of China (82370777)

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:

探索性研究/预试验 

Study phase:

0

研究设计:

析因分组(即根据危险因素或暴露因素分组) 

Study design:

Factorial 

研究目的:

基于尿液微生态寻找新的生物标志物,构建新的诊断模型,辅助PSA4~10ng/ml区间的患者的临床诊断,减少患者接受不必要的有创检测,减少医疗资源的浪费。  

Objectives of Study:

Based on the urine microecology, we seek new biomarkers and construct new diagnostic models to assist in the clinical diagnosis of patients in the PSA range of 4 to 10 ng/ml, reduce the number of patients undergoing unnecessary invasive tests, and reduce the waste of medical resources.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

门诊诊断为PSA升高的患者

Inclusion criteria

Patients with an outpatient diagnosis of elevated PSA

排除标准:

1、本次入院后 复测的PSA数值不在4-10范围内的样本 ; 2、近3个月内使用抗生素的样本; 3、同时患有尿路感染的样本; 4、有其他肿瘤病史的样本; 5、在研究中途退出的患者。

Exclusion criteria:

1. Patients with retested PSA values outside 4-10ng/ml range after admission were excluded; 2. Patients who had used antibiotics in the past 3 months were excluded; 3. Patients with urinary tract infection were excluded; 4. Patients with other tumors were excluded; 5. Patients who dropped out of the study were excluded.

研究实施时间:

Study execute time:

From 2023-11-01 00:00:00 To 2025-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2023-11-30 00:00:00 To 2025-12-31 00:00:00

干预措施:

Interventions:

组别:

前列腺癌组

样本量:

33

Group:

PCa group

Sample size:

干预措施:

干预措施代码:

Intervention:

none

Intervention code:

组别:

良性前列腺增生组

样本量:

42

Group:

BPH group

Sample size:

干预措施:

干预措施代码:

Intervention:

none

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

江苏 

市(区县):

 

Country:

China

Province:

Jiangsu

City:

单位(医院):

江南大学附属中心医院 

单位级别:

三甲 

Institution
hospital:

Jiangnan University Medical Center

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

总前列腺特异性抗原

指标类型:

主要指标

Outcome:

Total Prostate Specific Antigen

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

尿液微生物5R16S检测结果

指标类型:

主要指标

Outcome:

Urine microbiota 5R16S test results

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血清蛋白质检测结果

指标类型:

主要指标

Outcome:

Serum protein test results

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血清代谢物检测结果

指标类型:

主要指标

Outcome:

Serum metabolite test results

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:

中段尿

组织:

Sample Name:

midstream urine

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

标本中文名:

血液

组织:

Sample Name:

blood

Tissue:

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:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 40 years
最大 Max age 95 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):

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:

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

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):

预计于2027年6月共享原始数据,邮件联系研究负责人合理获取。

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

Expected to share raw data in June 2027, contact the research leader via email for reasonable access.

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:

通过HIS管理系统采集数据,以及管理保存数据。

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

Collect data through HIS management system, manage and save data.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2024-12-09 15:20:17