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注册号: Registration number: |
ChiCTR2600121279 |
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最近更新日期: Date of Last Refreshed on: |
2026-03-27 15:52:01 |
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注册时间: Date of Registration: |
2026-03-27 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: |
瞼板腺功能障礙的代謝組學研究 |
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Public title: |
Metabolomics study in meibomian gland dysfunction |
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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: |
瞼板腺功能障礙的代謝組學研究 |
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Scientific title: |
Metabolomics study in meibomian gland dysfunction |
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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: |
Jennifer Tsoi |
研究负责人: |
朱偉傑 |
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Applicant: |
Jennifer Tsoi |
Study leader: |
CHU Wai Kit |
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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 5860 |
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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: |
waikit@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: |
香港九龍旺角亞皆老街147K香港眼科醫院3樓 |
研究负责人通讯地址: |
香港九龍旺角亞皆老街147K香港眼科醫院4樓 |
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Applicant address: |
3/F, Hong Kong Eye Hospital, 147K Argyle Street, Kowloon, Hong Kong SAR |
Study leader's address: |
4/F, Hong Kong Eye Hospital, 147K Argyle Street, Kowloon, Hong Kong SAR |
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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: |
香港中文大學眼科與視覺科學系 |
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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: |
香港中文大學眼科與視覺科學系 |
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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: |
2025.719 |
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: |
香港中文大學–新界東醫院聯網 臨床研究倫理 聯席委員會 |
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Name of the ethic committee: |
Joint Chinese University of Hong Kong-New Territories East Cluster Clinical Research Ethics Committee |
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伦理委员会批准日期: Date of approved by ethic committee: |
2026-01-27 00:00:00 | ||
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伦理委员会联系人: |
Ms Envy Lee |
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Contact Name of the ethic committee: |
Ms Envy Lee |
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伦理委员会联系地址: |
香港沙田威爾斯親王醫院呂志和臨床醫學大樓8樓 |
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Contact Address of the ethic committee: |
8/F, Lui Che Woo Clinical Sciences Building, Prince of Wales Hospital, Shatin, Hong Kong |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+852 3505 3935 |
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 (DOVS), Chinese University of Hong Kong |
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研究实施负责(组长)单位地址: |
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 |
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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: |
醫療衞生研究基金 (HMRF) |
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Source(s) of funding: |
Health and Medical Research Fund |
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研究疾病: |
瞼板腺功能障礙 |
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Target disease: |
Meibomian gland dysfunction |
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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: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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研究设计: |
病例对照研究 |
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Study design: |
Case-Control study |
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研究目的: |
1)确认睑板腺功能障碍(MGD)患者和健康受试者的眼部病变状况。2)研究香港本地MGD患者的睑脂代谢组学。3)研究代谢物与睑板腺及眼表参数的相关性。 |
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Objectives of Study: |
1. Confirm the ophthalmopathy status of the MGD patients and healthy subjects. 2. Study the meibum metabolomics in local Hong Kong MGD patients. 3. Study the correlations of metabolites with meibomian gland and ocular surface parameters. |
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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: |
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Inclusion criteria |
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排除标准: |
瞼板腺功能障礙(MGD)患者與對照組: (1) 研究期间或研究开始前 3 个月内佩戴隐形眼镜; (2) 研究期间或研究开始前 3 个月内使用已知会影响睑板腺功能障碍 (MGD) 的局部用药(包括抗青光眼药、环孢素、抗生素、类固醇)或全身用药; (3) 已知會影響瞼板腺功能障礙或眼部疾病(包括甲狀腺眼疾、復發性結膜炎、眼部過敏)的严重全身性疾病(例如乾燥症)、皮膚病(例如酒渣鼻); (4) 研究期间或研究开始前 3 个月内进行眼部手术(不包括单纯性白内障手术),以及研究期间进行任何眼部手术; (5) 研究期间或研究开始前 6 个月内接受皮肤科治疗[包括眼周和面部区域的化学剥脱、激光、强脉冲光 (IPL) 或能量设备治疗]; (6) IPL治療的禁忌症(包括近期曬傷、光敏感、活動性或色素性皮膚病變、癌症、植入物、刺青、眼周半永久化妝); (7) 懷孕、哺乳、計劃懷孕或有生育能力但未使用可靠避孕方法的婦女; (8) 雙眼淚膜破裂時間(TFBUT)>10秒; (9) 存在眼睑病变和位置异常,包括眼睑肿胀、眼睑皮肤松弛、睑内翻、睑外翻、睫毛下垂和眼睑闭合不全。 |
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Exclusion criteria: |
MGD patients and the control group: (1) Contact lens wear 3 months before or during the study period; (2) Use of topical (including anti-glaucomatous, cyclosporin, antibiotics, steroid) or systemic medication known to affect (worsen or improve) MGD 3 months before or during the study period; (3) Major systemic (e.g. Sjogren’s syndrome), dermatologic (e.g. Rosacea) known to affect MGD or ocular conditions (including thyroid eye disease, recurrent conjunctivitis, ocular allergies); (4) Ocular procedures (excluding uncomplicated cataract operation) 3 months before and any ocular procedure during the study period; (5) Dermatological treatment [including chemical peeling, laser, intense pulsed light (IPL) or energy device in the periocular and facial region] 6 months before or during the study period; (6) Contraindications to IPL therapy (including recent sun-burn, photosensitivity, active or pigmented skin lesions, cancer, implants, tattoos, semi-permanent makeup in the periocular area; (7) Women who are pregnant, nursing, planning pregnancy, or of childbearing potential not using a reliable method of contraception; (8) Tear breakup time (TFBUT)>10 seconds in both eyes; (9) Presence of eyelid pathologies and malposition including eyelid swelling, dermatochalasis, entropion, ectropion, lash ptosis and lagophthalmos. |
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研究实施时间: Study execute time: |
从 From 2026-04-01 00:00:00至 To 2028-03-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-04-01 00:00:00 至 To 2027-03-31 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: |
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Blinding: |
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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): |
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: |
我們將非常謹慎地處理患者數據,確保不以任何形式侵犯患者的隱私。個人資料將以匿名方式保存,研究文件中的代碼無法被識別,並將遵循醫管局關於處理患者資料隱私的政策。為保護病患隱私,所有研究資料將依照醫管局/醫院關於處理/儲存/銷毀病患病歷的政策進行處理。數據將被鎖在部門/病房保存病人機密資訊的櫃子中。電子資料將保存在醫院的安全電腦中,並設有存取權限。 USB 裝置不會用於儲存病患資訊或個人資料。香港身分證號碼僅用於跟進健康狀況以及在必要時查閱醫院管理局的病歷。所有收集的個人資料將嚴格保密,僅用於研究目的。我們將使用研究代碼。包含研究代碼和患者身份之間關聯信息的電子文件文檔不會包含任何其他信息,並將與研究數據文件或數據表分開保存,並採用與病歷同樣嚴格的安全措施。任何包含可識別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,按照同樣嚴格的安全規定進行處理。所有研究人員都將負責資料處理和保護。所有可識別的個人資料都將進行匿名化和加密處理,並遵循醫管局關於處理患者資料隱私的政策。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Patient data would be handled with utmost care taking care not to breach patient's privacy in any form. Personal data is kept anonymous with unidentifiable code on study document and will follow the HA policy on handling of patient data privacy. To protect patient privacy, all research data would be handled in line with HA/Hospital’s policy in handling/storage/destruction of patients’ medical records. They would be locked in cabinets where the department/ward keeps patients' confidential information. Electronic data would be saved in secured computer of the hospital with restricted access. USB Device would not be used for patient information nor personal data. The HKID number is only for the follow-up of health condition and review the medical records from Hospital Authority when necessary. All personal data collected will be kept strictly confidential and for research purpose only. 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 encrypted 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 |