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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: |
ChiCTR2300072394 |
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最近更新日期: Date of Last Refreshed on: |
2023-06-12 16:54:31 |
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注册时间: Date of Registration: |
2023-06-12 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: |
中国皮肤型红斑狼疮研究联盟狼疮患者队列研究 |
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Public title: |
A cohort study of patients with lupus erythematosus in Chinese population, from CCLCL |
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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: |
中国皮肤型红斑狼疮研究联盟( Chinese Cutaneous Lupus Collaborating League,CCLCL)狼疮患者队列研究 |
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Scientific title: |
A cohort study of patients with lupus erythematosus in Chinese population, from Chinese Cutaneous Lupus Collaborating League (CCLCL) |
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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: |
靳慧 |
研究负责人: |
陆前进 |
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Applicant: |
Hui Jin |
Study leader: |
QianJin Lu |
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申请注册联系人电话: Applicant telephone: |
+86 133 3773 3972 |
研究负责人电话:
Study leader's |
+86 137 8709 7676 |
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申请注册联系人传真 : Applicant Fax: |
+86 025 85478185 |
研究负责人传真: Study leader's fax: |
+86 025 85478185 |
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申请注册联系人电子邮件: Applicant E-mail: |
jin1010hui@126.com |
研究负责人电子邮件: Study leader's E-mail: |
qianlu5860@pumcderm.cams.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: |
江苏省南京市玄武区蒋王庙街道12号 |
研究负责人通讯地址: |
江苏省南京市玄武区蒋王庙街道12号 |
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Applicant address: |
No.12, Jiangwangmiao Street, Xuanwu District, Nanjing, Jiangsu Province, China |
Study leader's address: |
No.12, Jiangwangmiao Street, Xuanwu District, Nanjing, Jiangsu Province, 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: |
中国医学科学院 北京协和医学院 皮肤病医院(皮肤病研究所) |
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Applicant's institution: |
Hospital for skin diseases, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China |
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研究负责人所在单位: |
中国医学科学院 北京协和医学院 皮肤病医院(皮肤病研究所) |
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Affiliation of the Leader: |
Hospital for skin diseases, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China |
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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: |
(2023)临快审第(002)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: |
中国医学科学院皮肤病医院(研究所)医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Hospital for skin diseases, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-02-14 00:00:00 | ||
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伦理委员会联系人: |
聂瑾 |
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Contact Name of the ethic committee: |
Jin Nie |
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伦理委员会联系地址: |
江苏省南京市玄武区蒋王庙街12号 |
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Contact Address of the ethic committee: |
No.12, Jiangwangmiao Street, Xuanwu District, Nanjing, Jiangsu Province |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 25 8547 8037 |
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: |
中国医学科学院 北京协和医学院 皮肤病医院(皮肤病研究所) |
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Primary sponsor: |
Hospital for skin diseases, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China |
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研究实施负责(组长)单位地址: |
江苏省南京市玄武区蒋王庙街道12号中国医学科学院皮肤病医院 |
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Primary sponsor's address: |
No.12, Jiangwangmiao Street, Xuanwu District, Nanjing, Jiangsu Province |
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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: |
中国医学科学院医学与健康科技创新工程(重大协同创新项目)(2021-I2M-1-059) |
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Source(s) of funding: |
Medical and Health Science and Technology Innovation Project of Chinese Academy of Medical Sciences (Major Collaborative Innovation Project) (2021-I2M-1-059) |
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研究疾病: |
红斑狼疮 |
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Target disease: |
Lupus Erythematosus |
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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: |
流行病学研究 |
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Study type: |
Epidemilogical research |
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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: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
①建立可对红斑狼疮(lupus erythematosus, LE)相关皮肤表现进行系统记录、动态图片采集及管理的电子化LE登记管理系统; ②建立同时包含CLE和SLE、且可对狼疮相关皮肤表现动态监测和管理的多中心红斑狼疮患者队列——“中国皮肤型红斑狼疮研究联盟(Chinese Cutaneous Lupus Collaborating League,CCLCL)狼疮患者队列”; ③为CLE及SLE的诊疗、管理提供持续长久的真实世界数据。 |
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Objectives of Study: |
① To establish an electronic LE registration and management system for systematic recording, dynamic picture collection and management of skin manifestations related to lupus erythematosus (LE). ② To establish a multicenter lupus erythematosus patient cohort that includes both cutaneous LE (CLE) and systemic LE (SLE) and can dynamically monitor and manage lupus-related skin manifestations, the "lupus patient cohort of Chinese Cutaneous Lupus Collaborating League (CCLCL) ". ③Provide continuous and long-lasting real-world data for the diagnosis, treatment and management of CLE and SLE. |
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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年龄3岁及以上,性别不限; ②SLE患者纳入:符合2019年EULAR/ACR SLE分类标准或2012年SLICC SLE分类标准中任意一项即可纳入。 ③CLE患者纳入:参考Asian Dermatological Association (ADA) 皮肤型红斑狼疮诊断、治疗、长期监测指南(2021),综合考虑患者的临床表现和组织病理学特点,临床确诊为任意类型的CLE的患者。包括急性皮肤型红斑狼疮(Acute cutaneous lupus erythematosus,ACLE)、亚急性皮肤型红斑狼疮(Subacute cutaneous lupus erythematosus,SCLE)、慢性皮肤型红斑狼疮(CCLE)。其中ACLE可分为局限性、泛发性两个亚型;SCLE可分为环形红斑型、丘疹鳞屑型两个亚型;CCLE可分为局限性盘状红斑狼疮(Discoid lupus erythematosus,DLE)、播散性盘状红斑狼疮(Disseminated discoid lupus erythematosus,DDLE)、疣状红斑狼疮(Verrucous lupus erythematosus,VLE)、肿胀性红斑狼疮(Tumid lupus erythematosus,TLE)、深在性红斑狼疮(lupus erythematosus profundus,LEP)、冻疮样红斑狼疮(Chilblain lupus erythematosus,CHLE)、Blaschko线状红斑狼疮(Blaschko linear lupus erythematosus,BLLE) 多个亚型。 ④签署知情同意书,自愿参加本项目并能按要求完成访谈评估及留取血样本。 |
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Inclusion criteria |
① Age 3 years and above, regardless of gender. ② Inclusion of patients with SLE: meeting either the 2019 EULAR/ACR SLE classification criteria or the 2012 SLICC SLE classification criteria will be included. ③ Inclusion of patients with CLE: Referring to the Asian Dermatological Association (ADA) guidelines for the diagnosis, treatment, and long-term monitoring of cutaneous lupus erythematosus (2021), patients with any type of CLE, which were clinically diagnosed by considering the clinical and histopathological features of the patients. Including acute cutaneous lupus erythematosus (ACLE), subacute cutaneous lupus erythematosus (SCLE), and chronic cutaneous lupus erythematosus (CCLE). ACLE can be divided into two subtypes: limited and generalized; SCLE can be divided into two subtypes: annular erythematous and papulosquamous; CCLE can be divided into limited discoid lupus erythematosus (DLE), disseminated discoid lupus (DDLE), Verrucous lupus erythematosus (VLE), Tumid lupus erythematosus (TLE), lupus erythematosus profundus (LEP), Chilblain lupus erythematosus (CHLE), and Blaschko linear lupus erythematosus (BLLE). ④ Sign the informed consent form, voluntarily participate in this project and be able to complete the interview assessment and take blood samples as required. |
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排除标准: |
①存在精神异常或视力、听力障碍等妨碍问卷调查正常进行的因素; |
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Exclusion criteria: |
① There are some factors that hinder the normal conduct of the questionnaire, such as mental abnormalities, visual or hearing impairments and so on. ② Refuse to participate in the process of informed consent. |
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研究实施时间: Study execute time: |
从 From 2023-06-15 00:00:00至 To 2033-06-15 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-06-15 00:00:00 至 To 2033-06-15 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): |
N/A |
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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): |
不涉及共享原始数据 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
No sharing of raw data involved |
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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: |
在医渡云医学技术有限公司(无外资背景)的技术支持下,建立电子化红斑狼疮登记系统(自己建立专属电子采集和管理系统,EDC),可在手机端和电脑端收集和管理患者人口学资料、病程、就诊和治疗资料。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
With the technical support of MeduCloud Medical Technology Co., Ltd (with no foreign investment background), an electronic lupus erythematosus registration system is established (Set up our own Electronic Data Capture, EDC), which allows the collection and management of patient demographic data, disease course, consultation and treatment information on mobile phones and computers. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |