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注册号: Registration number: |
ChiCTR-ROC-17011816 |
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最近更新日期: Date of Last Refreshed on: |
2017-06-30 16:35:09 |
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注册时间: Date of Registration: |
2017-06-30 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: |
非干预性脓毒症患者免疫状态研究 |
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Public title: |
observational study of immune status in patients with sepsis |
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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: |
非干预性脓毒症患者免疫状态研究 |
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Scientific title: |
observational study of immune status in patients with sepsis |
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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: |
陈上仲 |
研究负责人: |
严静 |
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Applicant: |
Chen Shangzhong |
Study leader: |
Yan Jin |
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申请注册联系人电话: Applicant telephone: |
+86 18814882081 |
研究负责人电话:
Study leader's |
+86 18814882081 |
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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: |
csz19871103@126.com |
研究负责人电子邮件: Study leader's E-mail: |
296066337@qq.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
http://zjhospital.com.cn |
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: |
浙江省杭州市西湖区龙井路黄泥岭38号 |
研究负责人通讯地址: |
浙江省杭州市西湖区灵隐路12号 |
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Applicant address: |
38 Longjin Road, Xihu District, Hangzhou, Zhejiang, China |
Study leader's address: |
12 Linying Road, Xihu District, Hangzhou, Zhejiang, China |
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申请注册联系人邮政编码: Applicant postcode: |
310017 |
研究负责人邮政编码: Study leader's postcode: |
310017 |
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申请人所在单位: |
浙江医院 |
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Applicant's institution: |
Zhejiang Hospital |
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研究负责人所在单位: |
浙江医院 |
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Affiliation of the Leader: |
Zhejiang Hospital |
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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: |
2016-1K |
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: |
浙江医院医学伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of ZheJiang Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2016-04-15 00:00:00 | ||
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伦理委员会联系人: |
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Contact Name of the ethic committee: |
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伦理委员会联系地址: |
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Contact Address of the ethic committee: |
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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: |
浙江医院 |
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Primary sponsor: |
Zhejiang Hospital |
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研究实施负责(组长)单位地址: |
浙江省杭州市西湖区灵隐路12号 |
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Primary sponsor's address: |
12 Linying Road, Xihu District, Hangzhou, Zhejiang, 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: |
赛生医药(中国)有限公司 |
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Source(s) of funding: |
Sciclone pharmaceuticals (China) Co. Ltd. |
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研究疾病: |
脓毒症 |
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Target disease: |
sepsis |
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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: |
病因学/相关因素研究 |
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Study type: |
Cause/Relative factors 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: |
单臂 |
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Study design: |
Single arm |
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研究目的: |
本研究期望通过深入观察脓毒症发生发展过程中免疫状态的变化;探索不同免疫指标在脓毒症发生发展中的作用,为脓毒症规范化诊治提供免疫学依据。 |
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Objectives of Study: |
Objective to observe the changes of immune status and the role of different immune indexes in the course of sepsis development.And to provide an immunological basis for the standardized diagnosis and treatment of sepsis in immunization. |
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药物成份或治疗方案详述: |
采用多中心观察性研究,通过对ICU中所有入选的的成年脓毒症患者进行观察性研究,分别于入选时、第1、2、3、5、7、14天和第28天后收集相关免疫学指标,并收集相关的临床资料及预后指标,从而分析脓毒症发生发展过程中免疫细胞、免疫因子的变化情况以及与脓毒症预后的相关性。 |
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Description for medicine or protocol of treatment in detail: |
Multicenter observational study was used in this study. The related immunological indexes and clinical data were collected at the time of 1,2,3,5,7,14 and 28 days after sepsis. |
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纳入标准: |
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Inclusion criteria |
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排除标准: |
1.拒绝签署知情同意书者; |
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Exclusion criteria: |
1. Patients or family members do not agree to participate in the trial; |
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研究实施时间: Study execute time: |
从 From 2017-07-01 00:00:00至 To 2019-07-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2017-07-01 00:00:00 至 To 2019-07-01 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): |
非随机分组 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
it is not a randomize trial |
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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 |
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): |
Not stated |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Not stated |
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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: |
Not stated |
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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: |