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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: |
ChiCTR2500112656 |
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最近更新日期: Date of Last Refreshed on: |
2025-11-18 09:11:40 |
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注册时间: Date of Registration: |
2025-11-18 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: |
赛立奇单抗治疗中重度银屑病的多中心临床综合评价 |
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Public title: |
A Comprehensive Multicenter Clinical Evaluation of Xeligekimab in the Treatment of Moderate-to-Severe Psoriasis |
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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: |
赛立奇单抗治疗中重度银屑病的多中心临床综合评价 |
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Scientific title: |
A Comprehensive Multicenter Clinical Evaluation of Xeligekimab in the Treatment of Moderate-to-Severe Psoriasis |
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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: |
王禹毅 |
研究负责人: |
刁庆春/王琴 |
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Applicant: |
Wang Yuyi |
Study leader: |
Diao Qingchun/Wang Qin |
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申请注册联系人电话: Applicant telephone: |
+86 138 8324 0312 |
研究负责人电话:
Study leader's |
+86 139 8373 5555 |
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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: |
wangyuyi188@126.com |
研究负责人电子邮件: Study leader's E-mail: |
wangyuyi188@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: |
重庆市渝中区道门口40号 |
研究负责人通讯地址: |
重庆市渝中区道门口40号 |
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Applicant address: |
40 Daomenkou, Yuzhong District, Chongqing |
Study leader's address: |
40 Daomenkou, Yuzhong District, Chongqing |
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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: |
重庆市中医院 |
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Applicant's institution: |
Chongqing Hospital of Traditional Chinese Medicine |
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研究负责人所在单位: |
重庆市中医院 |
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Affiliation of the Leader: |
Chongqing Hospital of Traditional Chinese Medicine |
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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-KY-HY-13 |
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: |
重庆市中医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Chongqing Hospital of Traditional Chinese Medicine |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-06-23 00:00:00 | ||
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伦理委员会联系人: |
杨洋 |
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Contact Name of the ethic committee: |
Yang Yang |
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伦理委员会联系地址: |
重庆市江北区盘溪七支路6号 |
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Contact Address of the ethic committee: |
6 7th Branch of Panxi Road, Jiangbei District, Chongqing |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 67630637 |
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: |
重庆市中医院 |
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Primary sponsor: |
Chongqing Hospital of Traditional Chinese Medicine |
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研究实施负责(组长)单位地址: |
重庆市渝中区道门口40号 |
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Primary sponsor's address: |
40 Daomenkou, Yuzhong District, Chongqing |
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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: |
重庆市卫健委 |
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Source(s) of funding: |
Chongqing Health Commission |
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研究疾病: |
中重度银屑病 |
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Target disease: |
Moderate-to-Severe Psoriasis |
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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: |
连续入组 |
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Study design: |
Sequential |
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研究目的: |
本研究旨在全面、系统地综合评价赛立奇单抗在真实世界中银屑病患者群体中的应用效果。通过多维度的分析,深入探究该方案的有效性、安全性和经济性,为临床医生和药师提供科学准确的用药指导,促进药品的合理使用,推动药品研发和生产的科学性与可持续发展。 |
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Objectives of Study: |
This study aims to conduct a comprehensive and systematic evaluation of the real-world effectiveness of Xeligekimab in an integrative treatment model for patients with psoriasis. Through multidimensional analysis, it seeks to thoroughly investigate the regimen's efficacy, safety, and cost-effectiveness. The findings are intended to provide clinicians and pharmacists with scientific and evidence-based guidance, promote rational drug use, and support scientifically sound and sustainable drug development and production. |
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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≥18岁,性别不限; 2.符合中重度银屑病诊断; 3.经研究者评估,适合初次使用赛立奇单抗治疗的患者; 4.自愿参加并签署知情同意书者。 |
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Inclusion criteria |
1. Age >= 18 years, male or female; 2.Diagnosed with moderate to severe plaque psoriasis 3.Considered by the investigator to be a candidate for initial treatment with Xeligekimab 4.Voluntary participation and signed informed consent form. |
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排除标准: |
1.筛选或基线时,为药物性银屑病(如β受体阻滞剂、钙通道阻滞剂或锂盐引起的新发银屑病或银屑病加重等); 2.伴有其他炎症性疾病,包括但不限于:炎症性肠病等,并经研究者判断可能会影响疗效及安全性评估; 3.正在接受治疗或未接受治疗的恶性肿瘤患者 4.对赛立奇单抗注射液的活性成分或任何辅料产生严重超敏反应的 5.重要临床意义的活动性感染 6.妊娠或哺乳期女性 7.具有严重精神病史或家族史者 8.其他合并说明书禁忌症的患者 9.其他原因研究者认为不合适参加本研究者 |
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Exclusion criteria: |
1.Drug-induced psoriasis at screening or baseline (e.g., psoriasis onset or exacerbation due to beta-blockers, calcium channel blockers, lithium, etc.); 2.Presence of other inflammatory diseases, including but not limited to inflammatory bowel disease, which in the investigator’s judgment may affect efficacy or safety assessments; 3.Patients with currently treated or untreated malignant tumors; 4.History of severe hypersensitivity to the active ingredient or any excipient of Setokimab injection; 5.Active infection of clinical significance; 6.Pregnant or lactating women; 7.History of severe psychiatric disorder or family history thereof; 8.Patients with other contraindications as per the prescribing information; 9.Any other condition considered by the investigator to make the patient unsuitable for participation. |
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研究实施时间: Study execute time: |
从 From 2025-06-01 00:00:00至 To 2027-06-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-12-01 00:00:00 至 To 2027-04-01 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: |
公开/Public |
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盲法: |
无 |
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Blinding: |
None |
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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 |
是Yes |
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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): |
本研究中去标识化的参与者数据可在文章发表后向合理请求的研究人员开放。提案需发送至通讯作者邮箱,经审查批准后,请求方需签署数据使用协议后方可获得数据。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Deidentified participant data will be made available upon reasonable request to the corresponding author, following publication. Proposals should be directed to [email address]. Requestors will need to sign a data access agreement. |
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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: |
1.数据采集:本研究仅使用病例报告表(CRF)记录和汇总数据。所有源数据由经过培训的研究中心人员在每次访视期间直接填写至纸质CRF表中。 2.数据管理:基于CRF的数据管理流程包括: (1)填写: 研究人员及时将方案要求的所有数据点记录在CRF中 (2)核查: site协调员对CRF的完整性和可读性进行初步质量检查 (3)质疑管理: 通过直接与研究人员沟通澄清任何数据差异或缺失问题 (4)汇总: 所有CRF数据经人工整理汇编至中央汇总表 (5)验证: 随机抽取部分数据与源文件进行比对核查,确保数据准确性 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
1.Data Collection: All study data were exclusively recorded and aggregated using Case Report Forms (CRFs). Source data were directly transcribed into paper CRFs by trained site investigators during each study visit. 2.Data Management: The CRF-based data management process included: (1)Completion: Investigators documented all protocol-required data points in the CRFs contemporaneously (2)Verification: Site coordinators performed initial quality checks for completeness and legibility (3)Query Resolution: Any discrepancies or missing data were clarified through direct communication with investigators (4)Aggregation: All CRF data were manually compiled into centralized summary tables (5)Validation: Random spot-checks were conducted against source documents to verify data accuracy |
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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 |