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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: |
ChiCTR2500115291 |
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最近更新日期: Date of Last Refreshed on: |
2025-12-24 15:17:35 |
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注册时间: Date of Registration: |
2025-12-24 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
人工智能辅助的青霉素及头孢类药物过敏皮肤试验判读研究 |
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Public title: |
Research on the Interpretation of Skin Tests for Penicillin and Cephalosporin Allergies Assisted by Artificial Intelligence |
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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: |
基于卷积神经网络的β-内酰胺类抗菌药物皮肤试验结果辅助诊断模型的构建 |
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Scientific title: |
Skin test results of β-lactam antibiotics based on convolutional neural network Construction of auxiliary diagnostic model |
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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: |
徐亦虹 |
研究负责人: |
潘红英 |
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Applicant: |
Xu Yihong |
Study leader: |
Pan Hongying |
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申请注册联系人电话: Applicant telephone: |
+86 19858118820 |
研究负责人电话: Study leader's telephone: |
+86 571 86006396 |
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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: |
xuyihong@zju.edu.cn |
研究负责人电子邮件: Study leader's E-mail: |
panhy@srrsh.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: |
中国浙江省杭州市上城区庆春东路3号 |
研究负责人通讯地址: |
中国浙江省杭州市上城区庆春东路3号 |
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Applicant address: |
3 Qingchun East Road, Shangcheng District, Hangzhou, Zhejiang ,China |
Study leader's address: |
3 Qingchun East Road, Shangcheng District, Hangzhou, Zhejiang ,China |
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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: |
浙江大学医学院附属邵逸夫医院 |
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Applicant's institution: |
Sir Run Run Shaw Hospital,Zhejiang University School of Medicine |
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研究负责人所在单位: |
浙江大学医学院附属邵逸夫医院 |
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Affiliation of the Leader: |
Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University |
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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: |
邵逸夫医院伦审2024研第0453号 |
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: |
浙江大学医学院附属邵逸夫医院医学伦理委员会 |
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Name of the ethic committee: |
Ethics Committee,Sir Run Run Shaw Hospital,Zhejiang University School of Medicine |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-08-09 00:00:00 |
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伦理委员会联系人: |
杨漾池 |
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Contact Name of the ethic committee: |
Yang Yangchi |
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伦理委员会联系地址: |
中国浙江省杭州市上城区庆春东路3号 |
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Contact Address of the ethic committee: |
3 Qingchun East Road, Shangcheng District, Hangzhou, Zhejiang ,China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 571 86006811 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
yyc261@foxmail.com |
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研究实施负责(组长)单位: |
浙江大学医学院附属邵逸夫医院 |
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Primary sponsor: |
Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University |
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研究实施负责(组长)单位地址: |
中国浙江省杭州市上城区庆春东路3号 |
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Primary sponsor's address: |
3 Qingchun East Road, Shangcheng District, Hangzhou, Zhejiang ,China |
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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: |
自选课题(自筹) |
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Source(s) of funding: |
Self-funded |
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Target disease: |
Skin test for beta-lactam antibiotics |
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Target disease code: |
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研究类型: |
诊断试验 |
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Study type: |
Diagnostic test |
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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: |
诊断试验诊断准确性 |
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Study design: |
Diagnostic test for accuracy |
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研究目的: |
1.基于 CNN 技术,构建一个准确高效的β-内酰胺类抗菌药物皮肤试验辅助诊断模型。 2.利用混淆矩阵和内部验证,对本研究中的诊断模型进行验证和评价。 |
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Objectives of Study: |
1. Based on CNN technology, an accurate and efficient auxiliary diagnostic model for skin tests of β-lactam antibacterial drugs is constructed.2. The diagnostic model in this study is verified and evaluated by using confusion matrix and internal validation. |
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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.在急诊科进行β-内酰胺类抗菌药物皮肤试验的患者。 |
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Inclusion criteria |
1.Patients undergoing skin tests for beta-lactam antibiotics in the emergency department. 2.Volunteer to participate in the study and sign the informed consent. If the subject is unable to read and sign due to incapacity or other reasons Informed consent, or if the subject is a minor, the guardian must represent the informed process and sign the informed consent. If the subject does not have the ability to read the informed consent form (e.g., illiterate subjects), the informed process must be witnessed and signed by a witness Informed consent. |
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排除标准: |
1.危重患者。 |
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Exclusion criteria: |
1. Subjects voluntarily withdrew from the study.2.The investigator believes that the subjects are not suitable to participate in this study. |
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研究实施时间: Study execute time: |
从 From 2024-09-01 00:00:00至 To 2026-06-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2024-09-02 00:00:00 至 To 2025-12-20 00:00:00 |
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诊断试验: Diagnostic Tests: |
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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: |
结束 /Completed |
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 |
Yes |
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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): |
在研究结束后6个月内,在ResMan平台进行数据共享。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Data sharing will be conducted on the ResMan platform within six months after the completion of the research. |
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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: |
数据通过研究人员采集并进行保管 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
The data were collected by the researchers and then stored. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |