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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: |
ChiCTR2500096782 |
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最近更新日期: Date of Last Refreshed on: |
2025-02-06 15:03:03 |
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注册时间: Date of Registration: |
2025-02-06 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: |
一项非介入性多中心数据的回顾性研究,旨在描述坏疽性脓皮病(PG)患者的临床特征、诊断标准和治疗需求 |
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Public title: |
A retrospective study of non-interventional multicenter data was conducted to describe the clinical characteristics, diagnostic criteria, and treatment needs of patients with pyoderma gangrenosum (PG) |
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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: |
一项非介入性多中心数据的回顾性研究,旨在描述坏疽性脓皮病(PG)患者的临床特征、诊断标准和治疗需求 |
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Scientific title: |
A retrospective study of non-interventional multicenter data was conducted to describe the clinical characteristics, diagnostic criteria, and treatment needs of patients with pyoderma gangrenosum (PG) |
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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: |
方姗 |
研究负责人: |
乔建军 方姗 |
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Applicant: |
Shan Fang |
Study leader: |
Jianjun Qiao Shan Fang |
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申请注册联系人电话: Applicant telephone: |
+86 195 5012 1827 |
研究负责人电话:
Study leader's |
+86 137 3554 2393 |
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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: |
fangshan520w@163.com |
研究负责人电子邮件: Study leader's E-mail: |
qiaojianjun@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: |
浙江省杭州市庆春路79号 |
研究负责人通讯地址: |
浙江省杭州市庆春路79号 |
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Applicant address: |
79 Qingchun Road, Hangzhou 310003, Zhejiang, China |
Study leader's address: |
79 Qingchun Road, Hangzhou 310003, Zhejiang, China |
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申请注册联系人邮政编码: Applicant postcode: |
200443 |
研究负责人邮政编码: Study leader's postcode: |
200443 |
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申请人所在单位: |
浙江大学医学院附属第一医院 |
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Applicant's institution: |
The First Affiliated Hospital of Zhejiang University School of Medicine |
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研究负责人所在单位: |
浙江大学医学院附属第一医院 |
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Affiliation of the Leader: |
The First Affiliated Hospital of Zhejiang University School of 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: |
浙大一院伦审2024研第1415号-快 |
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: |
浙江大学医学院附属第一医院IIT伦理审查委员会 |
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Name of the ethic committee: |
Clinical Reserach Ethics Committee of the First Affiliated Hospital Zhejiang University School of Medicine |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-12-06 00:00:00 | ||
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伦理委员会联系人: |
厉丽丽 |
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Contact Name of the ethic committee: |
lili li |
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伦理委员会联系地址: |
浙江省杭州市庆春路79号 |
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Contact Address of the ethic committee: |
79 Qingchun Road, Hangzhou 310003, Zhejiang, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 571 8723 3418 |
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: |
浙江大学医学院附属第一医院 |
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Primary sponsor: |
The First Affiliated Hospital of Zhejiang University School of Medicine |
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研究实施负责(组长)单位地址: |
浙江省杭州市庆春路79号 |
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Primary sponsor's address: |
The First Affiliated Hospital of Zhejiang University School of Medicine |
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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: |
中国自然科学基金 |
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Source(s) of funding: |
National Natural Science Foundation of China |
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研究疾病: |
坏疽性脓皮病 |
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Target disease: |
pyoderma gangrenosum |
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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: |
回顾性研究 | ||||||||||||||||||||||
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Study phase: |
Retrospective study |
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研究设计: |
横断面 |
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Study design: |
Cross-sectional |
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研究目的: |
研究主要目的: 评估3类PG诊断标准的一致性和实用性 研究次要目的: 描述PG患者人口统计学特征和疾病临床特征 统计治疗方案的选择和疗效 |
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Objectives of Study: |
The main objective of the study is: To evaluate the consistency and practicality of three types of PG diagnostic criteria. The secondary objectives of the study are: To describe the demographic characteristics and clinical features of PG patients. To count the selection and efficacy of treatment plans. |
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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、符合坏疽性脓皮病诊断的患者;2、接受治疗及随访的患者;3、病历信息和临床资料完整。 |
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Inclusion criteria |
1. Patients meeting the diagnostic criteria for pyoderma gangrenosum. 2. Patients who received treatment and follow-up. 3. Complete medical records and clinical data. |
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排除标准: |
1、诊断不明确的患者;2、病历信息和临床资料不完整的患者。 |
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Exclusion criteria: |
1. Patients with unclear diagnosis. 2. Patients with incomplete medical records and clinical data. |
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研究实施时间: Study execute time: |
从 From 2025-02-07 00:00:00至 To 2025-06-07 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-02-07 00:00:00 至 To 2025-06-07 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): |
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: |
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Blinding: |
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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): |
2025年6月7日以后随文章发表在https://www.newwa.cn/center/project/projectManage公布 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Published with the article after June 7th, 2025 at https://www.newwa.cn/center/project/projectManage |
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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: |
病历表收集患者信息后在国内NEWWA电子采集和管理系统进行数据管理 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
We use case Record Form to collect patient information and then manages the data in the NEWWA electronic capture and management system(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 |