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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: |
ChiCTR2200065218 |
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最近更新日期: Date of Last Refreshed on: |
2022-11-01 08:17:20 |
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注册时间: Date of Registration: |
2022-11-01 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: |
超分子水杨酸治疗玫瑰痤疮的有效性及安全性评价临床研究方案 |
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Public title: |
A clinical study protocol to evaluate the efficacy and safety of supramolecular salicylic acid in the treatment of rosacea |
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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: |
超分子水杨酸治疗玫瑰痤疮的有效性及安全性评价 |
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Scientific title: |
Evaluation of efficacy and safety of supramolecular salicylic acid in the treatment of rosacea |
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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: |
张骞 |
研究负责人: |
蒋献 |
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Applicant: |
Qian Zhang |
Study leader: |
Xian Jiang |
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申请注册联系人电话: Applicant telephone: |
15828107909 |
研究负责人电话:
Study leader's |
028-85423319 |
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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: |
zhangqian.97@foxmail.com |
研究负责人电子邮件: Study leader's E-mail: |
jennyxianj@163.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: |
中华人民共和国四川省成都市武侯区国学巷37号 |
研究负责人通讯地址: |
中华人民共和国四川省成都市武侯区国学巷37号 |
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Applicant address: |
NO.37 Guo Xue Xiang, Wuhou District, Chengdu, Sichuan, China |
Study leader's address: |
NO.37 Guo Xue Xiang, Wuhou District, Chengdu, Sichuan, 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: |
四川大学华西医院 |
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Applicant's institution: |
West China Hospital, Sichuan University |
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研究负责人所在单位: |
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Affiliation of the Leader: |
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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: |
2019年审(1177)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: |
四川大学华西医院生物医学伦理审查委员会 |
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Name of the ethic committee: |
Ethics Committee on Biomedical Research, West China Hospital of Sichuan University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2020-03-19 00:00:00 | ||
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伦理委员会联系人: |
邓绍林 |
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Contact Name of the ethic committee: |
Shaolin Deng |
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伦理委员会联系地址: |
中华人民共和国四川省成都市武侯区国学巷37号 |
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Contact Address of the ethic committee: |
NO.37 Guo Xue Xiang, Wuhou District, Chengdu, Sichuan, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 28 85423237 |
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: |
四川大学华西医院 |
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Primary sponsor: |
West China Hospital, Sichuan University |
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研究实施负责(组长)单位地址: |
中华人民共和国四川省成都市武侯区国学巷37号 |
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Primary sponsor's address: |
NO.37 Guo Xue Xiang, Wuhou District, Chengdu, Sichuan, 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: |
上海瑞志医药科技有限公司 |
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Source(s) of funding: |
Shanghai Ruizhi Pharmaceutical Technology Co., Ltd |
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研究疾病: |
玫瑰痤疮 |
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Target disease: |
Rosacea |
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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: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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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: |
采用安慰剂对照,评估超分子水杨酸治疗玫瑰痤疮的有效性和安全性 |
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Objectives of Study: |
To evaluate the efficacy and safety of supramolecular salicylic acid compared with placebo control in the treatment of rosacea |
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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)根据美国玫瑰痤疮协会最新诊断标准(2017版)-附件1确诊的以丘疹脓疱为主要表型的患者; |
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Inclusion criteria |
1) Patients with papulopustular rosacea as a major phenotype according to Standard classification and pathophysiology of rosacea: The 2017 update by the National Rosacea Society Expert Committee (Annex 1); |
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排除标准: |
1)面部患有其他皮肤疾病,如黄褐斑、雀斑和脂溢性皮炎而可能影响对试验结果的判断; |
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Exclusion criteria: |
1) Patients with other facial skin diseases such melisma, freckles and asseborrheic dermatitis, which may affect the determination of the study results; |
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研究实施时间: Study execute time: |
从 From 2020-03-19 00:00:00至 To 2022-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2020-03-19 00:00:00 至 To 2022-12-31 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: |
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): |
采用中心和玫瑰痤疮严重程度分层区组随机化法。由第四军医大学卫生统计学教研室专业人员应用SAS统计软件PLAN过程步骤,根据试验组数、中心个数以及各中心病例分配数设置区组长度等参数,程序化生成随机编码表,并完成药物编盲。受试者根据就诊顺序和随机编码表分配试验用药,随机进入试验组和安慰剂组。临床试验的随机编码表称为盲底,待药品编盲结束后,盲底一式两份密封分别保存在申办者和组长单位临床试验机构。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Stratified block randomization was used based on the rosacea severity. Professionals from the Department of Health Statistics of the Fourth Military Medical University applied the PLAN procedure in SAS statistical software to set parameters such as block length upon the number of study groups, the number of cen |
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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: |
本试验为双盲研究,受试者和研究者不可区分所用药物的组别。数据管理和统计分析将在盲态下进行。 |
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Blinding: |
This trial is a double-blind study, and the subjects and researchers cannot distinguish the groups of drugs used. Data management and statistical analysis will be conducted in a blind state. |
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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): |
2023.12前通过里恩临床试验电子数据采集系统共享原始数据(https://www.rh-clinical.com) |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Share IPD through Riehen Clinical Trial Management System before Oct. 2023 (https://www.rh-clinical.com/) |
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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: |
病例记录表,电子采集和管理系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form,Electronic Data Capture |
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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 |