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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: |
ChiCTR2400080231 |
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最近更新日期: Date of Last Refreshed on: |
2024-01-24 14:28:21 |
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注册时间: Date of Registration: |
2024-01-24 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: |
**[已更正] 请合并上传所有伦理批件(初审/复审+修正案);研究负责人和批件不完全一致,请完善;请确认征募开始日期(首例知情签署日期)+征募结束(最后一例出组日期)+研究结束(完成统计分析)+主、次要测量指标+样本量+数据采集和管理方式; 前瞻性先導研究:運用人工智能(AI)分析光學相干斷層掃描(OCT)影像以辦認眼疾並協助分流篩查 |
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Public title: |
Using an artificial intelligence based optical coherence tomography image analysis for eye disease identification to support triage screening: a prospective pilot study |
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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: |
前瞻性先導研究:運用人工智能(AI)分析光學相干斷層掃描(OCT)影像以辦認眼疾並協助分流篩查 |
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Scientific title: |
Using an artificial intelligence based optical coherence tomography image analysis for eye disease identification to support triage screening: a prospective pilot study |
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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: |
Ms Jennifer Tsoi |
研究负责人: |
張艷蕾副教授 / 譚智勇教授 |
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Applicant: |
Ms Jennifer Tsoi |
Study leader: |
Dr Cheung Yim Lui Carol / Prof Tham Chee Yung Clement |
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申请注册联系人电话: Applicant telephone: |
+852 3943 5818 |
研究负责人电话:
Study leader's |
+852 3943 5831 |
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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: |
jennifertsoi@cuhk.edu.hk |
研究负责人电子邮件: Study leader's E-mail: |
carolcheung@cuhk.edu.hk |
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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: |
九龍亞皆老街147K號 香港眼科醫院3樓 |
研究负责人通讯地址: |
九龍亞皆老街147K號香港眼科醫院4樓 |
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Applicant address: |
3/F, Hong Kong Eye Hospital, 147K Argyle Street, Kowloon |
Study leader's address: |
4/F, Hong Kong Eye Hospital, 147K Argyle Street, Kowloon |
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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: |
香港中文大學眼科及視覺科學學系 |
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Applicant's institution: |
Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong |
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研究负责人所在单位: |
香港中文大學眼科及視覺科學學系 |
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Affiliation of the Leader: |
Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong |
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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: |
KC/KE-20-0241/ER-1 |
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: |
九龍中及九龍東聯網臨床研究倫理委員會 |
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Name of the ethic committee: |
Research Ethics Committee (Kowloon Central / Kowloon East) |
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伦理委员会批准日期: Date of approved by ethic committee: |
2020-11-26 00:00:00 | ||
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伦理委员会联系人: |
Ms Lyon Chan |
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Contact Name of the ethic committee: |
Ms Lyon Chan |
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伦理委员会联系地址: |
香港九龍加士居道30號伊利沙伯醫院護士宿舍4樓414室 |
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Contact Address of the ethic committee: |
Room 414, Nurse Quarters, Queen Elizabeth Hospital, 30 Gascoigne Road, Kowloon, Hong Kong |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+852 3506 8888 |
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: |
香港中文大學眼科及視覺科學學系 |
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Primary sponsor: |
Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong |
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研究实施负责(组长)单位地址: |
香港九龍亞皆老街147K號香港眼科醫院3樓 |
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Primary sponsor's address: |
3/F, Hong Kong Eye Hospital, 147K Argyle Street, Kowloon, Hong Kong |
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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: |
部門經費 |
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Source(s) of funding: |
Departmental fund |
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研究疾病: |
與視網膜和視神經頭相關的眼疾(例如糖尿病黃斑水腫、青光眼和其他視網膜異常) |
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Target disease: |
Eye diseases related to retina and optic nerve head (e.g., DME, glaucoma, and other retinal abnormalities) |
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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: |
诊断试验 |
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Study type: |
Diagnostic test |
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研究所处阶段: |
诊断试验新技术临床试验 | ||||||||||||||||||||||
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Study phase: |
Diagnostic New Technique Clincal Study |
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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: |
本研究旨在為評估AI輔助系統於自動評估OCT影像質素的表現、從OCT影像辨認出與視網膜及視神經相關的眼疾(例如糖尿病黃斑水腫、青光眼和其他視網膜疾病),並提供臨床分流建議,以協助現實中對眼睛疾病之分流篩查。 |
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Objectives of Study: |
The current project aims to assess the performance of the AI-assisted system prospectively for automatically assessing image quality, identifying eye diseases related to retina and optic nerve (e.g. DME, glaucoma, and other retinal abnormalities) from OCT images, and providing a clinical triage suggestion to support real-world eye disease triage screening. |
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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: |
因以下原因而從篩檢計畫、初級保健機構或其他診所轉介至香港眼科醫院分流處的參與者: 1) 任何糖尿病眼部疾病(例如糖尿病黃斑水腫、糖尿病視網膜病變); 或 2) 任何視網膜異常(例如老年黃斑部病變、視網膜前膜、黃斑裂孔); 或 3) 患有明確青光眼或有青光眼相關可疑發現的參與者(例如視杯與視盤比率增加、眼壓升高、視盤出血和視網膜神經纖維層變薄)。 |
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Inclusion criteria |
Subjects presenting to the Triage Unit of the Hong Kong Eye Hospital who are referred from screening programmes or primary care settings or other clinics to see ophthalmologists for the following reasons: 1) any diabetic eye diseases (e.g. diabetic macular edema, diabetic retinopathy); or 2) any retinal abnormalities (e.g. age-related macular degeneration, epiretinal membrane, macular hole); or 3) subjects with definite glaucoma or with glaucoma-related suspicious findings (e.g. increased cup to disc ratio, increased intraocular pressure, disc hemorrhage, and retinal nerve fibre layer thinning). |
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排除标准: |
接受OCT檢查有困難。 |
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Exclusion criteria: |
Subjects who have difficulty receiving OCT examinations. |
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研究实施时间: Study execute time: |
从 From 2020-11-01 00:00:00至 To 2024-10-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2021-02-01 00:00:00 至 To 2023-10-19 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: |
正在进行 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): |
無 |
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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 |
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): |
研究發表後半年上傳至ResMan(www.medresman.org.cn) |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Upload the research to ResMan (www.medrescman. org. cn) half a year after publication |
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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: |
將使用市面上 OCT設備對所有參與者進行雙眼視盤和黃斑立方體掃描。 OCT 掃描後,原始影像資料(例如 Cirrus OCT 中的 IMG 格式)將立即從 OCT 資料庫中提取到特定位置。資料將自動傳輸到GPU伺服器由AI輔助系統進一步處理。 收集的其他數據:針孔視力、眼底攝影、基線人口統計(例如種族、性別、吸煙)和全身病史(例如高血壓、糖尿病、高血脂)。 電子數據將只在我們安全的研究室電腦內保存,並受到密碼保護。這項研究的資料將給予香港中文大學醫學院眼科及視覺科學學系進行統計分析。參與者的身份將受嚴格保密,只有整體的結果將被公佈。個人資料將於研究完結後保存五年。於任何時間,參與者可要求銷毀所有相關的研究結果和記錄。如無需用於其他研究或治療,個人資料將於研究完成後保存5年。 我們將極為謹慎地處理患者數據,避免以任何形式侵犯患者的隱私。 為保障病人私隱,所有研究資料會依照醫院管理局/醫院處理/儲存/銷毀病人病歷的政策處理。 USB 裝置不會用於儲存病患資訊或個人資料。 個人資料(姓名、香港身分證、OPD/醫院號碼、地址及任何其他個人識別資料)不會記錄在項目的資料表或電子文件中。 將使用研究代碼來代替。 包含研究代碼和患者身份之間的連結資訊的電子文件文件不會包含任何其他信息,並且將與研究數據文件或數據表分開保存,具有與醫療記錄相同的嚴格安全性。任何包含個人識別資訊的文件或電子文件都將被視為醫療記錄的一部分,並將根據醫院政策遵守同樣嚴格的安全規定。所有調查人員將負責資料處理和保護。所有可辨識的個人資料均會匿名化,並遵守醫管局處理病人資料私隱的政策。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Optic disc and macular cube scans of both eyes will be performed for all recruited subjects using commercially available OCT devices. Raw image data (e.g. IMG format in Cirrus OCT) will be extracted from the OCT database to a specific location immediately after OCT scanning. The data will then be automatically transfer to a GPU server for further processing by the AI-assisted system. Other data collection at recruitment: Pinhole visual acuity, fundus photography, baseline demographics (e.g. ethnicity, gender, smoking) and systemic medical history (e.g. hypertension, diabetes, hyperlipidemia) will also be obtained. Electronic data will be only saved in physically-secured and password-protected computers in the research office of CUHK Eye Centre. Information from this study will be submitted to the Department of Ophthalmology & Visual Sciences, the Chinese University of Hong Kong for statistical analysis. Only the overall result will be published and subjects' identity will remain confidential. The signed consent form will be stored separately from interview notes and personal data to further protect confidentiality. Access to the data will be restricted to the researchers of this study. Records and results of all study investigations can be destroyed on subjects' request in future. Personal data will be kept for 5 years after study completion if not for further research or clinical use. Patient data would be handled with utmost care taking care not to breach patient's privacy in any form. To protect patient privacy, all research data would be handled in line with Hospital Authority / Hospital’s policy in handling / storage / destruction of patients’ medical records. USB Device would not be used for patient information nor personal data. Personal data (name, HKID, OPD / hospital numbers, address and any other personal identifiable information) would not be recorded on the project’s data sheets or electronic files. A study code would be used instead. The document of electronic file containing the linkage information between the study code and the identity of the patient would not contain any other information and would be kept separate from the study data files or data sheets with the same stringent security as the medical record. Any documents or electronic files containing personal identifiable information would be considered as part of the medical record and would be dealt with the same stringent regulations of security according to the hospital policies. All the investigators would be responsible for data handling and protection. All identifiable personal data will be anonymised and will follow the HA policy on handling of patient data privacy. |
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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 |