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注册号: Registration number: |
ChiCTR2500100029 |
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最近更新日期: Date of Last Refreshed on: |
2025-04-02 08:41:55 |
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注册时间: Date of Registration: |
2025-04-02 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: |
特应性皮炎诊疗新技术研发-特应性皮炎生物标记物的临床研究 |
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Public title: |
Research on New Diagnostic and Therapeutic Technologies for Atopic Dermatitis-Clinical Research on Biomarkers of Atopic Dermatitis |
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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: |
特应性皮炎诊疗新技术研发-特应性皮炎生物标记物的临床研究 |
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Scientific title: |
Research on New Diagnostic and Therapeutic Technologies for Atopic Dermatitis-Clinical Research on Biomarkers of Atopic Dermatitis |
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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: |
罗阳 |
研究负责人: |
姚煦 |
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Applicant: |
Luo Yang |
Study leader: |
Yao Xu |
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申请注册联系人电话: Applicant telephone: |
+86 158 5057 0361 |
研究负责人电话:
Study leader's |
+86 135 1251 3536 |
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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: |
luoyangsdnu@126.com |
研究负责人电子邮件: Study leader's E-mail: |
dryao_xu@126.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: |
江苏省南京市玄武区蒋王庙街12号 |
研究负责人通讯地址: |
江苏省南京市玄武区蒋王庙街12号 |
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Applicant address: |
12 Jiangwangmiao street, Nanjing, Jiangsu, China |
Study leader's address: |
12 Jiangwangmiao street, Nanjing, Jiangsu, 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: |
中国医学科学院皮肤病医院(中国医学科学院皮肤病研究所) |
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Applicant's institution: |
Hospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences, Peking Union Medical CollegeCollege |
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研究负责人所在单位: |
中国医学科学院皮肤病医院(中国医学科学院皮肤病研究所) |
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Affiliation of the Leader: |
Hospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences, Peking Union Medical College |
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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: |
(2024)临快审第(074)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: |
Ethics Committee of Dermatology Hospital, Chinese Academy of Medical Sciences |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-11-29 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: |
Nie Jin |
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伦理委员会联系地址: |
江苏省南京市蒋王庙街12号 |
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Contact Address of the ethic committee: |
12 Jiangwangmiao street, Nanjing, Jiangsu, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 25 8547 0673 |
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: |
中国医学科学院皮肤病医院(中国医学科学院皮肤病研究所) |
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Primary sponsor: |
Hospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences, Peking Union Medical College |
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研究实施负责(组长)单位地址: |
江苏省南京市蒋王庙街12号 |
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Primary sponsor's address: |
12 Jiangwangmiao street, Nanjing, Jiangsu, 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: |
中国医学科学院皮肤病医院高水平医院建设攻关任务 |
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Source(s) of funding: |
High-level Hospital Construction and Key Research Tasks of the Dermatology Hospital of Chinese Academy of Medical Sciences |
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研究疾病: |
特应性皮炎 |
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Target disease: |
Atopic dermatitis |
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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: |
建立高质量的包含1000-1500例AD患者临床数据库和生物样本库; 筛选与AD发病、病情、治疗及预后相关的生物标记物,构建数学模型,并在AD患者中进行验证。 |
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Objectives of Study: |
Establish a high-quality clinical database and biobank containing 1000-1500 cases of AD patients. Screen for biomarkers related to the onset, progression, treatment, and prognosis of AD, construct mathematical models, and validate them in AD patients. |
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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: |
1、患有恶性肿瘤或在筛选前5年内有恶性肿瘤病史; 2、存在可能干扰疗效评价的其他炎性皮肤疾病(如银屑病、副银屑病、嗜酸细胞增多性皮炎等); 3、严重心、脑、肺、肝、肾、血液等重要器官系统疾病,研究者认为不适宜参与本研究; 4、研究首次移植前4周内接受过系统应用糖皮质激素、雷公藤、环孢素等免疫抑制剂治疗,或3个月内接受过生物制剂(如度普利尤单抗、奥马珠单抗等); 5、4周内使用过抗微生物药物、益生菌/元制剂、调节肠道微生态治疗或其他显著影响肠道菌群的药物; 6、已知的活动性结核等活动性或复发性严重感染; 7、先天性免疫缺陷或先天性免疫力低下者; 8、吸毒、酗酒、精神异常或依从性差无法合作者; 9、备孕期妇女、孕妇及哺乳期妇女; 10、同时参加其他临床试验研究者; 11、研究者认为其他不宜参加的情况 |
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Exclusion criteria: |
1. Have a malignant tumor or a history of malignant tumor within 5 years before screening; 2. There are other inflammatory skin diseases that may interfere with the evaluation of efficacy (such as psoriasis, parapsoriasis, eosinophilic dermatitis, etc.); 3. Serious diseases of heart, brain, lung, liver, kidney, blood and other important organ systems, which the investigator considers inappropriate to participate in this study; 4. Received immunosuppressant therapy such as systemic glucocorticoids, tripterygium wilfordii, cyclosporine within 4 weeks before the first transplant of the study, or received biological agents (such as dupilumab, omalizumab, etc.) within 3 months; 5. Use of antimicrobial drugs, probiotics/meta preparations, intestinal microecological regulation therapy or other drugs that significantly affect the intestinal flora within 4 weeks; 6. Known active tuberculosis and other active or recurrent serious infections; 7. Those with congenital immunodeficiency or congenital immunodeficiency; 8. Drug abuse, alcoholism, mental abnormalities or poor compliance and inability to cooperate; 9. Women who are trying to get pregnant, pregnant women and lactating women; 10. Investigators who participate in other clinical trials at the same time; 11. Other circumstances that the researcher deems inappropriate to participate |
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研究实施时间: Study execute time: |
从 From 2024-05-01 00:00:00至 To 2026-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-04-07 00:00:00 至 To 2026-12-31 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): |
不共享。试验完成后的原始数据将通过luoyangsdnu@126.com进行上传,预计上传时间为课题结束后一年内,即2027年12月31日前。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Don't share. The raw data after the completion of the trial will be uploaded through the luoyangsdnu@126.com, which is expected to be uploaded within one year after the end of the project, i.e., before December 31, 2027. |
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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: |
所有数据录入病例记录表。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
All data will be kept in the case records form. |
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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 |