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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: |
ChiCTR2500103187 |
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最近更新日期: Date of Last Refreshed on: |
2025-05-26 16:46:36 |
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注册时间: Date of Registration: |
2025-05-26 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: |
以依拉环素为基础的联合方案对比最佳可用疗法治疗实体器官移植受者多重耐药菌感染的有效性和安全性:一项多中心、回顾观察性研究 |
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Public title: |
The efficacy and safety of elacyclin-based combination regimens compared with the best available therapy for multi-drug resistant bacterial infections in solid organ transplant recipients: A multicenter, retrospective observational study |
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注册题目简写: |
实体器官移植受者多重耐药菌感染治疗的有效性和安全性 |
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English Acronym: |
The efficacy and safety of the treatment for multi-drug resistant bacterial infections in recipients of solid organ transplantation |
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研究课题的正式科学名称: |
以依拉环素为基础的联合方案对比最佳可用疗法治疗实体器官移植受者多重耐药菌感染的有效性和安全性:一项多中心、回顾观察性研究 |
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Scientific title: |
The efficacy and safety of elacyclin-based combination regimens compared with the best available therapy for multi-drug resistant bacterial infections in solid organ transplant recipients: A multicenter, retrospective observational study |
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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: |
周茜 |
研究负责人: |
巨春蓉 |
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Applicant: |
Zhou Qian |
Study leader: |
Ju Chunrong |
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申请注册联系人电话: Applicant telephone: |
+86 156 2238 1986 |
研究负责人电话:
Study leader's |
+86 159 1576 1346 |
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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: |
87069560@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
juchunrong@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: |
中国广东省广州市荔湾区桥中中路28号 |
研究负责人通讯地址: |
中国广东省广州市荔湾区桥中中路28号 |
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Applicant address: |
No. 28, Qiaozhong Middle Road, Liwan District, Guangzhou City, Guangdong Province, China |
Study leader's address: |
No. 28, Qiaozhong Middle Road, Liwan District, Guangzhou City, Guangdong 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: |
广州医科大学附属第一医院大坦沙院区 |
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Applicant's institution: |
The Datansha Campus of the First Affiliated Hospital of Guangzhou Medical University |
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研究负责人所在单位: |
广州医科大学附属第一医院大坦沙院区 |
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Affiliation of the Leader: |
The Datansha Campus of the First Affiliated Hospital of Guangzhou Medical University |
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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: |
ES-2024-K198-01 |
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: |
广州医科大学附属第一医院科研项目审查伦理委员会 |
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Name of the ethic committee: |
Ethics Committee for Scientific Research Project Review of the First Affiliated Hospital of Guangzhou Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-12-05 00:00:00 | ||
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伦理委员会联系人: |
张晓露 |
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Contact Name of the ethic committee: |
Zhang Xiaolu |
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伦理委员会联系地址: |
广州市桥中中路28号 |
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Contact Address of the ethic committee: |
No. 28, Qiaozhong Zhong Road, Guangzhou |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 20 8156 6265 |
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: |
广州医科大学附属第一医院 |
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Primary sponsor: |
The First Affiliated Hospital of Guangzhou Medical University |
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研究实施负责(组长)单位地址: |
中国广东省广州市荔湾区桥中中路28号 |
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Primary sponsor's address: |
No. 28, Qiaozhong Middle Road, Liwan District, Guangzhou City, Guangdong Province, 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: |
北京生命绿洲公益服务中心 |
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Source(s) of funding: |
Beijing Life Oasis Public Welfare Service Center |
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研究疾病: |
实体器官移植受者多重耐药菌感染 |
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Target disease: |
Multi-drug resistant bacterial infection in recipients of solid organ transplantation |
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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: |
病例对照研究 |
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Study design: |
Case-Control study |
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研究目的: |
评估依拉环素为基础的联合方案对比最佳可用疗法治疗SOTR人群多重耐药菌感染的疗效及安全性。 |
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Objectives of Study: |
To evaluate the efficacy and safety of the combination regimen based on eracycline compared with the best available therapy in the treatment of multi-drug resistant bacterial infections in the SOTR population. |
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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)≥18周岁。 2)既往接受实体器官(肝、肾、肺、心)移植患者,且长期接受≥1种免疫抑制剂治疗(糖皮质激素、钙神经蛋白抑制剂、抗细胞增殖类、雷帕霉素靶蛋白抑制剂等)。 3)已知或高度怀疑多重耐药病原菌(MDR)感染。MDR符合《多重耐药菌医院感染预防与控制中国专家共识》中的定义。 4)以依拉环素或BAT为基础的联合方案作为一线治疗方案使用。 5)若依拉环素为基础的联合方案,需要治疗组患者需应用依拉环素≥4天。 6)病例临床结局完整,资料能满足治疗结局评价(临床结局,微生物学结局和综合疗效评价)。 |
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Inclusion criteria |
1. >=18 years old. 2. Patients who have received solid organ transplants (liver, kidney, lung, heart) in the past and have been treated with at least one type of immunosuppressant for a long time (such as glucocorticoids, calcaren inhibitors, anti-cell proliferation drugs, rapamycin target protein inhibitors, etc.). 3. Infections caused by known or highly suspected multi-drug resistant pathogenic bacteria (MDR). MDR conforms to the definition in the "Chinese Expert Consensus on the Prevention and Control of Nosocomial Infections Caused by Multi-Drug Resistant Bacteria". 4. Combination regimens based on eracycline or BAT are used as first-line treatment regimens. 5. If the combination regimen is based on elacycline, patients in the treatment group need to be treated with elacycline for ≥4 days. 6. The clinical outcomes of the cases were complete, and the data could meet the requirements for treatment outcome evaluation (clinical outcomes, microbiological outcomes, and comprehensive efficacy evaluation). |
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排除标准: |
1.单纯尿路或颅内感染。 2.培养药敏显示微生物病原体对依拉环素不敏感(参考ChinaCAST的MIC折点) |
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Exclusion criteria: |
1. Simple urinary tract or intracranial infection. 2. The culture drug sensitivity shows that the microbial pathogen is not sensitive to etracycline (refer to the MIC breakpoint of ChinaCAST). |
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研究实施时间: Study execute time: |
从 From 2025-06-01 00:00:00至 To 2026-06-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-06-01 00:00:00 至 To 2026-06-01 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: |
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: |
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 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Not share |
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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: |
未说明 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Not stated |
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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 |