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注册号: Registration number: |
ChiCTR1800015596 |
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最近更新日期: Date of Last Refreshed on: |
2018-04-11 14:42:55 |
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注册时间: Date of Registration: |
2018-04-11 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: |
万古霉素在严重感染患者中的药代动力学及个体化给药方案研究 |
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Public title: |
Pharmacokinetics and individualized dosing regimens of vancomycin in patients with severe infection |
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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: |
万古霉素在严重感染患者中的药代动力学及个体化给药方案研究 |
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Scientific title: |
Pharmacokinetics and individualized dosing regimens of vancomycin in patients with severe infection |
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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: |
邹琪 |
研究负责人: |
邹琪 |
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Applicant: |
Qi Zou |
Study leader: |
Qi Zou |
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申请注册联系人电话: Applicant telephone: |
+86 18955246090 |
研究负责人电话:
Study leader's |
+86 18955246090 |
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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: |
panzersas@163.com |
研究负责人电子邮件: Study leader's E-mail: |
panzersas@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: |
安徽省蚌埠市长淮路287号 蚌埠医学院第一附属医院 |
研究负责人通讯地址: |
安徽省蚌埠市长淮路287号 |
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Applicant address: |
287 Huai Road, Bengbu, Anhui, China |
Study leader's address: |
287 Huai Road, Bengbu, Anhui, 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: |
蚌埠医学院第一附属医院重症医学科 |
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Applicant's institution: |
Intensive medicine department, The First Affiliated Hospital of Bengbu Medical College |
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研究负责人所在单位: |
蚌埠医学院第一附属医院 |
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Affiliation of the Leader: |
Intensive medicine department, The First Affiliated Hospital of Bengbu 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: |
LW[2014]001 |
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: |
蚌埠医学院第一附属医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of the First Affiliated Hospital of Bengbu Medical College |
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伦理委员会批准日期: Date of approved by ethic committee: |
1990-01-01 00:00:00 | ||
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伦理委员会联系人: |
万魏 |
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Contact Name of the ethic committee: |
Wei Wang |
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伦理委员会联系地址: |
安徽省蚌埠市长淮路287号 蚌埠医学院第一附属医院 |
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Contact Address of the ethic committee: |
The First Affiliated Hospital of Bengbu Medical College, 287 Huai Road, Bengbu, Anhui, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
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: |
蚌埠医学院第一附属医院 |
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Primary sponsor: |
The First Affiliated Hospital of Bengbu Medical College |
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研究实施负责(组长)单位地址: |
蚌埠医学院第一附属医院 |
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Primary sponsor's address: |
287 Huai Road, Bengbu, Anhui, 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: |
院课题 |
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Source(s) of funding: |
Hospital subject |
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研究疾病: |
重症感染 |
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Target disease: |
Severe infection |
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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: |
病例对照研究 |
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Study design: |
Case-Control study |
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研究目的: |
比较接受万古霉素治疗的单纯重症感染组、肾功能不全组和CRRT治疗组血药浓度,分析其峰浓度和谷浓度,并在临床药师的指导下优化万古霉素的治疗方案,研究其不同个体和特定群体的药代动力学特点,分析在体内药代动力学过程的影响因素,及对临床预后的影响。 |
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Objectives of Study: |
The blood concentration of simple severe infection group, renal failure group and CRRT group treated with vancomycin was compared, and its peak concentration and valley concentration were analyzed. Under the guidance of clinical pharmacists, the treatment scheme of vancomycin was optimized and the pharmacokinetic characteristics of different and specific groups were studied, and the pharmacokinetics in vivo was analyzed. The influencing factors of the process and the effect on clinical prognosis. |
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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.对糖肽类抗菌药物过敏者。2.存在听力功能减退者。3.孕妇或者围产期妇女。4.严重肾功能不全患者。 |
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Exclusion criteria: |
1. allergic to glycopeptide antibiotics; |
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研究实施时间: Study execute time: |
从 From 2015-01-01 00:00:00至 To 2018-03-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2015-01-01 00:00:00 至 To 2018-03-31 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: |
结束 /Completed |
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): |
N/A |
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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 |
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): |
中国临床试验注册中心 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Chinese clinical trial registry |
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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 |
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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, CRF |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |