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注册号: Registration number: |
ChiCTR2400089338 |
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最近更新日期: Date of Last Refreshed on: |
2024-09-06 09:00:01 |
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注册时间: Date of Registration: |
2024-09-06 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: |
依拉环素治疗中性粒细胞缺乏伴发热患者的疗效和安全性观察:一项基于HIS数据的多中心回顾性队列研究 |
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Public title: |
The efficacy and safety observation study of Eravacycline treatment in patients with neutropenia and fever: A multicenter retrospective cohort study based on HIS data |
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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: |
依拉环素治疗中性粒细胞缺乏伴发热患者的疗效和安全性观察:一项基于HIS数据的多中心回顾性队列研究 |
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Scientific title: |
The efficacy and safety observation study of Eravacycline treatment in patients with neutropenia and fever: A multicenter retrospective cohort study based on HIS data |
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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: |
杨栋林 |
研究负责人: |
冯四洲 |
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Applicant: |
Donglin Yang |
Study leader: |
Sizhou Feng |
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申请注册联系人电话: Applicant telephone: |
+86 22 2360 8592 |
研究负责人电话:
Study leader's |
+86 22 2360 8592 |
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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: |
yangdonglin@ihcams.ac.cn |
研究负责人电子邮件: Study leader's E-mail: |
szfeng@ihcams.ac.cn |
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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: |
天津市和平区南京路288号 |
研究负责人通讯地址: |
天津市和平区南京路288号 |
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Applicant address: |
288 Nanjing Road, Heping District, Tianjin |
Study leader's address: |
288 Nanjing Road, Heping District, Tianjin |
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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: |
中国医学科学院血液病医院(血液学研究所) |
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Applicant's institution: |
Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College |
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研究负责人所在单位: |
中国医学科学院血液病医院(血液学研究所) |
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Affiliation of the Leader: |
Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and 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: |
QTJC2024024-EC-1 |
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: |
中国医学科学院血液病医院伦理审查委员会 |
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Name of the ethic committee: |
Ethics Committee of Blood Diseases 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: |
2024-05-11 00:00:00 | ||
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伦理委员会联系人: |
王启柔 |
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Contact Name of the ethic committee: |
Qirou Wang |
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伦理委员会联系地址: |
天津市和平区南京路288号 |
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Contact Address of the ethic committee: |
288 Nanjing Road, Heping District, Tianjin |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 22 2390 9095 |
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: |
中国医学科学院血液病医院(血液学研究所) |
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Primary sponsor: |
Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College |
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研究实施负责(组长)单位地址: |
天津市和平区南京路288号 |
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Primary sponsor's address: |
288 Nanjing Road, Heping District, Tianjin |
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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 Service Center |
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研究疾病: |
粒细胞缺乏伴发热 |
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Target disease: |
Granulocyte deficiency with fever |
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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: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
主要研究目的: 观察依拉环素治疗中性粒细胞缺乏伴发热患者的疗效; 次要研究目的: 观察依拉环素治疗中性粒细胞缺乏伴发热患者的安全性; 描述接受依拉环素治疗中性粒细胞缺乏伴发热患者的特征; 描述依拉环素在中性粒细胞缺乏伴发热患者中的处方情况; 探索性研究目的: 探索不同亚组中性粒细胞缺乏伴发热患者的预后差异; |
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Objectives of Study: |
Main objective: To observe the therapeutic effect of Eravacycline on patients with neutropenia and fever; Secondary objectives: To observe the safety of Eravacycline treatment in patients with neutropenia and fever; To describe the characteristics of patients with neutropenia and fever receiving Eravacycline treatment; To describe the prescription situation of Eravacycline in patients with neutropenia and fever; Exploratory objective: To explore the prognostic differences among different subgroups of patients with neutropenia and fever; |
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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) 明确为单一铜绿假单胞菌所致的中性粒细胞缺乏伴发热。 2) 孕妇及哺乳期女性患者建议研究者根据临床实际情况选择。 |
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Exclusion criteria: |
1) Clearly identified as neutropenia accompanied by fever caused by a single strain of Pseudomonas Aeruginosa. 2) Pregnant women and nursing mothers are advised that the investigator should choose based on the actual clinical situation. |
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研究实施时间: Study execute time: |
从 From 2023-08-01 00:00:00至 To 2024-12-27 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-09-16 00:00:00 至 To 2024-12-27 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): |
N/A |
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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): |
不共享原始数据 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Not share the study source data. |
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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: |
EDC,CRF |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
EDC, CRF |
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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 |