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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: |
ChiCTR2600124249 |
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最近更新日期: Date of Last Refreshed on: |
2026-05-09 11:02:37 |
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注册时间: Date of Registration: |
2026-05-09 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: |
人工智能赋能增强CT辅助胰腺疾病患者精准管理决策的多中心临床研究 |
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Public title: |
A Multicenter Clinical Study on AI-Powered Precision Decision-Making Management for Pancreatic Diseases Using Contrast-Enhanced CT |
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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: |
人工智能赋能增强CT辅助胰腺疾病患者精准管理决策的多中心临床研究 |
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Scientific title: |
A Multicenter Clinical Study on AI-Powered Precision Decision-Making Management for Pancreatic Diseases Using Contrast-Enhanced CT |
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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: |
王蓓蕾 |
研究负责人: |
金钢 |
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Applicant: |
Wang Beilei |
Study leader: |
Jin Gang |
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申请注册联系人电话: Applicant telephone: |
+86 13774238083 |
研究负责人电话:
Study leader's |
+86 21 31161628 |
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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: |
lilly_wang@126.com |
研究负责人电子邮件: Study leader's E-mail: |
jingang@smmu.edu.cn |
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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: |
上海市杨浦区长海路168号 |
研究负责人通讯地址: |
上海市杨浦区长海路168号 |
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Applicant address: |
No. 168 Changhai Road, Yangpu District, Shanghai |
Study leader's address: |
No. 168, Changhai Road, Yangpu 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: |
海军军医大学第一附属医院 |
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Applicant's institution: |
The First Affiliated Hospital of Naval Medical University |
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研究负责人所在单位: |
海军军医大学第一附属医院 |
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Affiliation of the Leader: |
ShangHai ChangHai Hospital |
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是否获伦理委员会批准: |
是 |
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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: |
CHEC2025-411 |
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: |
上海长海医院医学伦理委员会 |
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Name of the ethic committee: |
Shanghai Changhai Hospital Medical Ethics Committee |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-10-17 00:00:00 | ||
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伦理委员会联系人: |
张优琴 |
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Contact Name of the ethic committee: |
Zhang Youqin |
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伦理委员会联系地址: |
上海市杨浦区长海路168号 |
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Contact Address of the ethic committee: |
No. 168, Changhai Road, Yangpu District, Shanghai |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 21 31162338 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
zhangyouqinzyq@sina.com |
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研究实施负责(组长)单位: |
海军军医大学第一附属医院 |
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Primary sponsor: |
ShangHai ChangHai Hospital |
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研究实施负责(组长)单位地址: |
上海市杨浦区长海路168号 |
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Primary sponsor's address: |
No. 168, Changhai Road, Yangpu 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: |
四大慢病重大专项 |
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Source(s) of funding: |
2025ZD0552300 |
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研究疾病: |
胰腺癌 |
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Target disease: |
pancreatic cancer |
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研究疾病代码: |
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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: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
本研究旨在开发并验证胰腺疾病智能决策分类系统,通过回顾性多中心数据评估其性能,并通过前瞻性临床试验验证其在真实临床场景中的分类准确性和应用价值。 |
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Objectives of Study: |
This study aims to develop and validate an intelligent decision-making classification system for pancreatic diseases. With the objectives of evaluating its performance on retrospective multicenter data and verifying its classification accuracy and application value in real-world clinical settings through a prospective clinical trial. |
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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: |
1.18-80 岁; 2.临床确诊为胰腺疾病; 3.有增强CT图像数据; 4.签署知情同意书,愿意参与研究。 |
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Inclusion criteria |
1. 18-80 years old; 2. Patients with a confirmed clinical diagnosis of pancreatic disease; 3. Patients with available contrast-enhanced CT scans; 4. Patients sign the informed consent form and agree to participate in the research. |
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排除标准: |
1.腹水、胰腺外伤、胸/腹部手术等原因导致图像质量不佳; |
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Exclusion criteria: |
1. Poor image quality caused by factors such as ascites, pancreatic trauma, thoracic/abdominal surgery, and other related conditions. 2. Unable to undergo contrast-enhanced CT due to contraindications such as a known allergy to iodinated contrast media or significant hepatic/renal dysfunction. 3. History of pancreatic surger; 4. Currently participating in another clinical trial; 5. Other conditions that, in the opinion of the investigator, would make the subject unsuitable for participation, include but are not limited to pregnant or lactating women, subjects with severe psychiatric disorders or cognitive impairment, subjects currently participating in or who have recently participated in another clinical trial, or subjects with significant medical conditions or complications that could interfere with the study results. |
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研究实施时间: Study execute time: |
从 From 2025-11-01 00:00:00至 To 2029-10-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-05-11 00:00:00 至 To 2029-10-31 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: |
不公开/Private |
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盲法: |
无 |
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Blinding: |
None |
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是否共享原始数据: IPD sharing |
否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): |
不共享 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Confidential |
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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: |
(1)数据收集:所有研究数据将通过电子问卷、电话询问、医院HIS系统或疾控癌症登记系统进行收集,包括患者基本信息、筛查结果、诊断结果、随访数据等; (2)数据存储:数据将存储在安全的服务器上,访问权限将严格限制在授权的研究人员和数据管理人员; (3)数据备份:定期进行数据备份,以防止数据丢失或损坏; 数据保密:所有数据均存储于研究单位的院内服务器,未经伦理委员会批准,严禁(4)以任何形式将数据移出研究单位。在数据分析前,对所有数据进行匿名化处理,确保无法通过数据直接或间接识别参与者身份。匿名化处理需遵循《信息安全技术个人信息安全规范》的要求,采用数据掩蔽、数据混淆等技术手段,确保处理后的信息无法复原。只有在获得伦理委员会明确批准的情况下,才允许对数据进行去匿名化处理,且去匿名化操作需严格限定在法律允许的范围内; (5)数据质量控制:定期进行数据清理和验证,确保数据的完整性和准确性。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
(1) Data Collection: All research data will be collected via electronic questionnaires, telephone interviews, hospital HIS (Hospital Information System) systems, or public health/disease control cancer registry systems. This includes patient demographic information, screening results, diagnostic results, follow-up data, and other relevant information.(2) Data Storage: Data will be stored on secure servers. Access will be strictly limited to authorized researchers and data management personnel.(3) Data Backup: Regular data backups will be performed to prevent data loss or corruption.(4) Data Confidentiality: All data will be stored on the research unit's internal servers. Without explicit approval from the Ethics Committee (or Institutional Review Board - IRB), it is strictly prohibited to move data out of the research unit in any form. Before data analysis, all data will be anonymized to ensure that participants' identities cannot be directly or indirectly identified through the data. Anonymization will adhere to the requirements of the "Information Security Technology - Personal Information Security Specification" (or relevant national standard), employing technical means such as data masking and data obfuscation to ensure that the processed information cannot be re-identified. De-anonymization will only be permitted with explicit approval from the Ethics Committee, and such de-anonymization operations must be strictly limited to what is legally permissible.(5) Data Quality Control: Regular data cleaning and validation will be performed to ensure data integrity and accuracy. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |