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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: |
ChiCTR2000040648 |
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最近更新日期: Date of Last Refreshed on: |
2020-12-06 00:43:39 |
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注册时间: Date of Registration: |
2020-12-06 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: |
轻中度主动脉瓣狭窄的多中心前瞻性队列研究 |
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Public title: |
Mild-to-moderate Aortic Stenosis cohort study |
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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: |
轻中度主动脉瓣狭窄的多中心前瞻性队列研究 |
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Scientific title: |
Mild-to-moderate Aortic Stenosis cohort 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: |
李子昂 |
研究负责人: |
张而立 |
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Applicant: |
Ziang Li |
Study leader: |
Erli Zhang |
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申请注册联系人电话: Applicant telephone: |
+86 19801117660 |
研究负责人电话: Study leader's telephone: |
+86 18500853301 |
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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: |
liziang@fuwaihospital.org |
研究负责人电子邮件: Study leader's E-mail: |
aricho1985@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: |
北京市西城区北礼士路167号 |
研究负责人通讯地址: |
北京市西城区北礼士路167号 |
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Applicant address: |
167 Lishi Road North, Xicheng District, Beijing, China |
Study leader's address: |
167 Lishi Road North, Xicheng District, Beijing, 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: |
阜外医院 |
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Applicant's institution: |
Fuwai Hospital |
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研究负责人所在单位: |
阜外医院 |
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Affiliation of the Leader: |
Fuwai Hospital |
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是否获伦理委员会批准: |
是/Yes |
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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: |
2020-1355 |
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: |
阜外医院伦理委员会 |
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Name of the ethic committee: |
ethics committee of Fuwai Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2013-08-26 00:00:00 |
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伦理委员会联系人: |
李立环 |
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Contact Name of the ethic committee: |
Lihuan Li |
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伦理委员会联系地址: |
北京市西城区北礼士路167号 |
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Contact Address of the ethic committee: |
167 Beilishi Lu, Xicheng District, Beijing, 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: |
阜外医院 |
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Primary sponsor: |
Fuwai Hospital |
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研究实施负责(组长)单位地址: |
北京市西城区北礼士路167号 |
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Primary sponsor's address: |
167 Lishi Road North, Xicheng District, Beijing, 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: |
中国医学科学院 |
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Source(s) of funding: |
Chinese Academy of Medical Sciences |
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Target disease: |
Aortic stenosis |
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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: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
这是针对轻中度主动脉瓣狭窄心脏病患者的发病、诊治、预后所进行的一项非干预性、多中心、前瞻性注册登记及队列研究。并同时建立我国成人主动脉瓣狭窄疾病注册登记系统,构建中国轻中度主动脉瓣狭窄患者数据库,建立基于网络的国际标准的主动脉瓣狭窄数据采集系统和多中心临床研究平台。 |
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Objectives of Study: |
This is a observational multicenter, prospective cohort study for adults with mild and moderate aortic stenosis. The purposes of this study were to evaluate the etiology clinical characteristics treatment modalities, and outcomes of patients with AS also to set up registration system of adult AS in China, to build a database of Chinese adult AS, to establish a web-based international standard data acquisition system for AS and a multicenter clinical research platform |
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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周岁以上 |
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Inclusion criteria |
1. Age ≥18 years |
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排除标准: |
1. 拒绝签署知情同意书的患者 |
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Exclusion criteria: |
1. patient who refuse to sign an informed consent |
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研究实施时间: Study execute time: |
从 From 2021-01-01 00:00:00至 To 2026-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2021-01-01 00:00:00 至 To 2021-12-31 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: |
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): |
NA |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
NA |
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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 |
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): |
论文形式发表 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
publish paper |
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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: |
病人的个体数据由各中心独立收集后通过电子数据收集(EDC)系统进行录入,其录入的模板已事先设计并分发于各中心。大多数数据都是临床研究中常见的数据。该研究具有多重的质量控制体系。各中心应妥善保管数据录入密匙,经通过培训的医学人员完成数据纳入。EDC 系统具有初步的质量监管功能,此外各中心分配有一个数据质量监管员。注册研究管理委员会将定期对于各中心纳入数据进行抽样检查。各中心将会事先接受数据纳入的培训,其中包括了对于患者事件及终点的明确定义。所有的新资料和信息会第一时间传递给研究相关人员。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Patient information is collected for research purposes only and confidentiality is strictly implemented. The clinical data of the participants is collected by each research center and entered into Electronic Data Capture (EDC) system in a previously agreed uniform format. The majority of the gathered information are common clinical data. This clinical trial has multiple quality control systems. The clinical data is strictly confidential and is gathered by trained medical professionals at each research center. In addition, each research center has a medical profesional monitoring the quality of the gathered data and data inspections are conducted by the Data Management Committee regularly. Before the beginning of the clinical trial, detailed training regarding data collection is also conducted at each research center. All first-hand data is uploaded and shared by the researchers as soon as possible. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |