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注册号: Registration number: |
ChiCTR-OOC-16009006 |
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最近更新日期: Date of Last Refreshed on: |
2016-08-10 13:53:57 |
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注册时间: Date of Registration: |
2016-08-10 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: |
行PCI术的冠心病患者登记研究 |
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Public title: |
A registration study of coronary heart disease patients undergoing PCI |
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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: |
冠心病患者PCI术后血小板反应差异的多因素研究 |
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Scientific title: |
Multifactors analysis of platelet reactivity variety in patiants with coronary heart disease after PCI |
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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: |
龚丽英 |
研究负责人: |
阳国平 |
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Applicant: |
Liying Gong |
Study leader: |
Guoping Yang |
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申请注册联系人电话: Applicant telephone: |
+86 13667307122 |
研究负责人电话:
Study leader's |
+86 13974817168 |
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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: |
gongliying1987@163.com |
研究负责人电子邮件: Study leader's E-mail: |
gpy9880@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: |
湖南省长沙市岳麓区桐梓坡路138号中南大学湘雅三医院 |
研究负责人通讯地址: |
湖南省长沙市岳麓区桐梓坡路138号中南大学湘雅三医院 |
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Applicant address: |
138 Tongzipo Road, Changsha, Hunan, China |
Study leader's address: |
138 Tongzipo Road, Changsha, Hunan, China |
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申请注册联系人邮政编码: Applicant postcode: |
410013 |
研究负责人邮政编码: Study leader's postcode: |
410013 |
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申请人所在单位: |
中南大学湘雅三医院 |
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Applicant's institution: |
The Third Xiangya Hospital of Central South University |
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研究负责人所在单位: |
中南大学湘雅三医院 |
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Affiliation of the Leader: |
The Third Xiangya Hospital of Central South 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: |
R15006 |
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: |
中南大学湘雅三医院伦理委员会医学伦理分委员会 |
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Name of the ethic committee: |
Institutional Review Board of The Third Xiangya Hospital,CSU |
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伦理委员会批准日期: Date of approved by ethic committee: |
2015-09-09 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: |
中南大学湘雅三医院 |
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Primary sponsor: |
The Third Xiangya Hospital of Central South University |
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研究实施负责(组长)单位地址: |
湖南省长沙市岳麓区桐梓坡路138号中南大学湘雅三医院 |
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Primary sponsor's address: |
138 Tongzipo Road, Changsha, Hunan, 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: |
特殊人群抗凝药物的个体化治疗的模型研究及应用 |
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Source(s) of funding: |
2014DFA30900 |
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研究疾病: |
冠心病 |
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Target disease: |
coronary heart disease |
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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: |
单臂 |
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Study design: |
Single arm |
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研究目的: |
以中国人群为研究对象的行PCI术的冠心病患者登记研究。获得该类患者PCI术后不良事件的发生率,明确不良反应发生的类型、表现形式、影响因素,从而建立风险管理流程,指导临床安全合理治疗,并为进一步深入研究提供基础与参考 |
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Objectives of Study: |
Study on the registration of coronary heart disease patients undergoing PCI in Chinese's population. Get the incidence of adverse events in these patients after PCI,a clear type of adverse reaction, forms, influencing factors, to establish risk management processes, clinical safety and reasonable treatment, and provide the basis for further research and reference. |
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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: |
无 |
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Exclusion criteria: |
no |
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研究实施时间: Study execute time: |
从 From 2015-09-09 00:00:00至 To 2018-09-09 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2015-09-16 00:00:00 至 To 2018-09-15 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): |
非随机对照研究 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Non randomized controlled study |
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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): |
通过ResMan查询原始数据2019.04 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
IPD will be public accessable via ResMan |
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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: |
我们入组的每个病人的原始数据均使用纸质版的CRF本保存,使用Epidata软件进行数据录入。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Each patient enrolled in our raw data use the paper version of the CRF of the storage, use Epidata software for data entry. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |