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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2400090699 |
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最近更新日期: Date of Last Refreshed on: |
2024-10-11 18:46:05 |
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注册时间: Date of Registration: |
2024-10-11 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
基于新型固相质谱技术的良性前列腺增生症体液代谢分子组多中心研究(BPH-FBI) |
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Public title: |
Multi-center study of Benign Prostate Hyperplasia Fluid Biomarker Investigation (BPH-FBI) |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
基于新型固相质谱技术的良性前列腺增生症体液代谢分子组多中心研究(BPH-FBI) |
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Scientific title: |
Multi-center study of Benign Prostate Hyperplasia Fluid Biomarker Investigation (BPH-FBI) |
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研究课题代号(代码): Study subject ID: |
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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: |
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申请注册联系人: |
谭海颂 |
研究负责人: |
徐斌 |
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Applicant: |
Tan Haisong |
Study leader: |
Xu Bin |
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申请注册联系人电话: Applicant telephone: |
+86 176 2115 7666 |
研究负责人电话: Study leader's telephone: |
+86 133 8627 1601 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
158374737@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
chxb2004@126.com |
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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): |
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申请注册联系人通讯地址: |
上海市黄浦区制造局路639号 |
研究负责人通讯地址: |
上海市黄浦区制造局路639号 |
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Applicant address: |
639 Zhizaoju Road, Huangpu District, Shanghai |
Study leader's address: |
639 Zhizaoju Road, Huangpu District, Shanghai |
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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: |
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申请人所在单位: |
上海交通大学医学院附属第九人民医院 |
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Applicant's institution: |
Shanghai Ninth People’s Hospital, Shanghai Jiaotong University School of Medicine |
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研究负责人所在单位: |
上海交通大学医学院附属第九人民医院 |
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Affiliation of the Leader: |
Shanghai Ninth People’s Hospital, Shanghai Jiaotong University School of Medicine |
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是否获伦理委员会批准: |
是/Yes |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
SH9H-2024-T202-2 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
上海交通大学医学院附属第九人民医院医学伦理委员会 |
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Name of the ethic committee: |
Ethic Committee of Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-07-25 00:00:00 |
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伦理委员会联系人: |
甄红 |
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Contact Name of the ethic committee: |
Zhen Hong |
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伦理委员会联系地址: |
上海市黄浦区制造局路639号 |
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Contact Address of the ethic committee: |
639 Zhizaoju Road, Huangpu District, Shanghai |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 21 2327 1699 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
上海交通大学医学院附属第九人民医院 |
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Primary sponsor: |
Shanghai Ninth People’s Hospital, Shanghai Jiaotong University School of Medicine |
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研究实施负责(组长)单位地址: |
上海市黄浦区制造局路639号 |
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Primary sponsor's address: |
639 Zhizaoju Road, Huangpu District, Shanghai |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
自筹 |
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Source(s) of funding: |
Self-raised |
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Target disease: |
Prostatic Hyperplasia |
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Target disease code: |
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研究类型: |
观察性研究 |
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Study type: |
Observational study |
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研究所处阶段: |
探索性研究/预试验 | ||||||||||||||||||||||
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Study phase: |
0 |
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研究设计: |
连续入组 |
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Study design: |
Sequential |
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研究目的: |
本研究为多中心临床研究,基于新型固相质谱技术分析良性前列腺增生患者与正常人群血、尿体液样本,结合临床常用病理参数及药物治疗情况进行分析,达到:1、辅助临床医生寻找良性前列腺增生体液特异性标志物;2、优化临床医生对前列腺增生患者药物治疗方案的制定;3、寻找针对良性前列腺增生的新治疗靶点。 |
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Objectives of Study: |
This study is a multicenter clinical research project that utilizes novel solid-phase mass spectrometry technology to analyze blood and urine samples from patients with benign prostatic hyperplasia and healthy individuals. The study, in conjunction with commonly used clinical pathological parameters and medication treatments, aims to achieve the following objectives: 1. Assist clinicians in identifying fluid-specific biomarkers for benign prostatic hyperplasia. 2. Optimize the formulation of medication treatment plans for patients with benign prostatic hyperplasia. 3. Identify new therapeutic targets for treating benign prostatic hyperplasia. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
良性前列腺增生:1、年龄≥50岁的患者;2、有明确的前列腺增生症状,符合前列腺增生诊断;3、观察对象充分理解患者须知,声明遵守研究程序,并签署知情同意书; 健康对照人群:1、无恶性肿瘤病史;2、无前列腺疾病相关病史;3、无重大基础疾病;4、观察对象充分理解患者须知,声明遵守研究程序,并签署知情同意书; |
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Inclusion criteria |
Benign Prostatic Hyperplasia (BPH) Group: 1. Patients aged 50 years or older. 2. Presence of clear symptoms of prostatic hyperplasia, meeting the diagnostic criteria for BPH. 3. Subjects fully understand the patient information, agree to adhere to the study procedures, and sign the informed consent form. Healthy Control Group: 1. No history of malignant tumors. 2. No history of prostate-related diseases. 3. No significant underlying diseases. 4. Subjects fully understand the patient information, agree to adhere to the study procedures, and sign the informed consent form. |
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排除标准: |
1、有恶性肿瘤相关病史;2、重大基础疾病病史患者; |
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Exclusion criteria: |
1. History of malignant tumors; 2. Patients with a history of significant underlying diseases. |
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研究实施时间: Study execute time: |
从 From 2024-11-01 00:00:00至 To 2025-10-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2024-11-01 00:00:00 至 To 2025-01-31 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
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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 |
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盲法: |
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Blinding: |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
No |
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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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None |
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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: |
病例记录表 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form, CRF |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |