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注册号: Registration number: |
ChiCTR2400084834 |
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最近更新日期: Date of Last Refreshed on: |
2024-05-27 08:40:12 |
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注册时间: Date of Registration: |
2024-05-27 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: |
和肽素结合高敏心肌肌钙蛋白对疑似非ST段抬高型心肌梗死(NSTEMI)患者的诊断价值评估 |
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Public title: |
Evaluation of the diagnostic value of copeptin combining with high-sensitivity cardiac troponin (hs-cTn) in patients with suspected non-ST-segment elevation myocardial infraction (NSTEMI) |
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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: |
和肽素结合高敏心肌肌钙蛋白对疑似非ST段抬高型心肌梗死(NSTEMI)患者的诊断价值评估 |
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Scientific title: |
Evaluation of the diagnostic value of copeptin combining with high-sensitivity cardiac troponin (hs-cTn) in patients with suspected non-ST-segment elevation myocardial infraction (NSTEMI) |
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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: |
陈东旭 |
研究负责人: |
宋振举 |
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Applicant: |
Chen.dongxu |
Study leader: |
Song.zhenju |
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申请注册联系人电话: Applicant telephone: |
+86 183 0184 4196 |
研究负责人电话:
Study leader's |
+86 183 0184 4196 |
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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: |
18301844196@sina.com |
研究负责人电子邮件: Study leader's E-mail: |
18301844196@sina.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: |
上海市徐汇区枫林路180号 |
研究负责人通讯地址: |
上海市徐汇区枫林路180号 |
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Applicant address: |
No. 180 Fenglin Road, Xuhui District, Shanghai |
Study leader's address: |
No. 180 Fenglin Road, Xuhui District, Shanghai |
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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: |
复旦大学附属中山医院 |
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Applicant's institution: |
Zhongshan Hospital Affiliated to Fudan University |
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研究负责人所在单位: |
复旦大学附属中山医院 |
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Affiliation of the Leader: |
Zhongshan Hospital Affiliated to Fudan 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: |
B2023-408 |
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: |
复旦大学附属中山医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Zhongshan Hospital, affiliated to Fudan University. |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-12-24 00:00:00 | ||
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伦理委员会联系人: |
樊嘉 |
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Contact Name of the ethic committee: |
Fan.jia |
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伦理委员会联系地址: |
上海市徐汇区枫林路180号 |
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Contact Address of the ethic committee: |
No. 180 Fenglin Road, Xuhui District, Shanghai |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 64041990 |
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: |
复旦大学附属中山医院 |
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Primary sponsor: |
Zhongshan Hospital Affiliated to Fudan University |
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研究实施负责(组长)单位地址: |
上海市徐汇区枫林路180号 |
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Primary sponsor's address: |
No. 180 Fenglin Road, Xuhui District, Shanghai |
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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: |
赛默飞世尔科技(中国)有限公司 |
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Source(s) of funding: |
Thermo Fisher Scientific |
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研究疾病: |
非ST段抬高型心肌梗死(NSTEMI) |
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Target disease: |
Non-ST Elevation Myocardial Infarction (NSTEMI) |
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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: |
诊断试验 |
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Study type: |
Diagnostic test |
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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: |
评估 DMS 法(copeptin 和 hs-cTn双指标阴性)快速识别中低风险疑似NSTEMI胸痛患者的有效性和安全性 |
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Objectives of Study: |
Evaluating the Efficacy and Safety of Utilizing the DMS Method (with Copeptin and hs-cTn as Biomarkers) for Expedited Identification of Middle- and Low-Risk Suspected NSTEMI patients with Chest Pain. |
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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、已明确为创伤性因素导致的胸痛。 2、心电图持续性ST段抬高,提示ST段抬高型心肌梗死(STEMI)。 3、严重肾功能不全,需要透析的晚期肾衰竭患者。 4、过去四周内有骨骼肌损伤或大手术的患者。 5、妊娠及哺乳期患者。 6、不能同意/不能理解知情同意书的患者。 |
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Exclusion criteria: |
1.Patients with chest pain due to trauma 2.The patient's electrocardiogram (ECG) reveals sustained elevation of the ST segment, indicative of a ST-elevation myocardial infarction (STEMI) 3.Severe renal insufficiency requiring dialysis in end-stage renal failure patients. 4.Patients who have suffered muscle injuries or undergone major surgery within the past four weeks. 5.Pregnant and lactating individuals 6.The informed consent form is not comprehensible or agreeable to patients |
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研究实施时间: Study execute time: |
从 From 2024-06-01 00:00:00至 To 2024-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-06-01 00:00:00 至 To 2024-12-31 00:00:00 |
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诊断试验: Diagnostic Tests: |
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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): |
本研究是队列研究,我们按照就诊顺序自然入组患者 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
This study is a cohort study.The patients are enrolled in a sequential order of presentation |
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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): |
可向研究者邮箱(18301844196@163.com)发送数据共享申请 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
The researcher's email (18301844196@163.com) is available for submission of a data sharing request |
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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: |
我们使用CRF表格记录数据,之后会将CRF表内的信息导入EDC系统中 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
The data is recorded in CRF tables, and subsequently imported into the Electronic Data Capture System |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |