|
注册号: Registration number: |
ChiCTR1900024152 |
|
最近更新日期: Date of Last Refreshed on: |
2019-06-28 11:40:46 |
|
注册时间: Date of Registration: |
2019-06-28 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
朱伟亮医师:该研究尚未获得伦理委员会批准。请于批准后再开始纳入参试者,并与我们联系上传批件。 别嘌呤醇对急性心肌梗死合并高尿酸血症患者的预后影响研究 |
|
Public title: |
The effect of allopurinol on the prognosis of patients with acute myocardial infarction with hyperuricemia |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
别嘌呤醇对急性心肌梗死合并高尿酸血症患者的预后影响研究 |
|
Scientific title: |
The effect of allopurinol on the prognosis of patients with acute myocardial infarction with hyperuricemia |
|
研究课题代号(代码): Study subject ID: |
|
|
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: |
|
申请注册联系人: |
朱伟亮 |
研究负责人: |
朱伟亮 |
|
Applicant: |
Zhu Weiliang |
Study leader: |
Zhu Weiliang |
|
申请注册联系人电话: Applicant telephone: |
+86 15711568281 |
研究负责人电话:
Study leader's |
+86 15711568281 |
|
申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
||
|
申请注册联系人电子邮件: Applicant E-mail: |
dimtarget@163.com |
研究负责人电子邮件: Study leader's E-mail: |
dimtarget@163.com |
|
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): |
||
|
申请注册联系人通讯地址: |
福建省厦门市湖里区金山路2999号 |
研究负责人通讯地址: |
福建省厦门市湖里区金山路2999号 |
|
Applicant address: |
2999 Jinshan Road, Huli District, Xiamen, Fujian, China |
Study leader's address: |
2999 Jinshan Road, Huli District, Xiamen, Fujian, China |
|
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: |
||
|
申请人所在单位: |
厦门大学附属心血管病医院 |
||
|
Applicant's institution: |
Xiamen Cardiovascular Hospital Xiamen University |
||
|
研究负责人所在单位: |
厦门大学附属心血管病医院 |
||
|
Affiliation of the Leader: |
Xiamen Cardiovascular Hospital Xiamen University |
||
|
是否获伦理委员会批准: |
否 |
||
|
Approved by ethic committee: |
No |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
伦理委员会批件附件: Approved file of Ethical Committee: |
||
|
批准本研究的伦理委员会名称: |
|
||
|
Name of the ethic committee: |
|
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2013-08-26 00:00:00 | ||
|
伦理委员会联系人: |
|
||
|
Contact Name of the ethic committee: |
|
||
|
伦理委员会联系地址: |
|
||
|
Contact Address of the ethic committee: |
|
||
|
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: |
||
|
研究实施负责(组长)单位: |
厦门大学附属心血管病医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Xiamen Cardiovascular Hospital Xiamen University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
福建省厦门市湖里区金山路2999号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
2999 Jinshan Road, Huli District, Xiamen, Fujian, China |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
厦门市科技计划项目 |
||||||||||||||||||||||
|
Source(s) of funding: |
Xiamen science and technology plan project |
||||||||||||||||||||||
|
研究疾病: |
急性心肌梗死合并高尿酸血症 |
||||||||||||||||||||||
|
Target disease: |
acute myocardial infarction with hyperuricemia |
||||||||||||||||||||||
|
研究疾病代码: |
|
||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||
|
研究类型: |
干预性研究 |
||||||||||||||||||||||
|
Study type: |
Interventional study |
||||||||||||||||||||||
|
研究所处阶段: |
上市后药物 | ||||||||||||||||||||||
|
Study phase: |
4 |
||||||||||||||||||||||
|
研究设计: |
随机平行对照 |
||||||||||||||||||||||
|
Study design: |
Parallel |
||||||||||||||||||||||
|
研究目的: |
明确别嘌呤醇对急性心肌梗死合并高尿酸血症患者预后、炎症状态影响,以及急性心肌梗患者使用别嘌呤醇的安全性。通过比较心血管病事件、再住院率、血栓栓塞、致死或非致死性心肌梗死、室性心律失常、致死性出血及大出血等发生率、炎症指标的改变、肝肾功能以及血常规等改变,明确别嘌呤醇对急性心肌梗死合并高尿酸血症患者预后、炎症状态影响,以及急性心肌梗患者使用别嘌呤醇的安全性,从而为急性心肌梗死患者降尿酸治疗提供数据支持,同时也提醒临床医生降尿酸治疗是冠心病危险因素控制的一个环节。 |
||||||||||||||||||||||
|
Objectives of Study: |
By comparing the cardiovascular events, and hospitalization, thromboembolism, fatal or nonfatal myocardial infarction, ventricular arrhythmia, the incidence of fatal bleeding and bleeding, inflammation, liver and kidney function and blood routine to clarify the effects of allopurinol on the prognosis and inflammatory status of patients with acute myocardial infarction and hyperuricemia. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
|||||||||||||||||||||||
|
Inclusion criteria |
|||||||||||||||||||||||
|
排除标准: |
1)妊娠患者; |
||||||||||||||||||||||
|
Exclusion criteria: |
1) pregnant patients; |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2020-01-01 00:00:00至 To 2024-08-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2020-01-01 00:00:00 至 To 2023-01-01 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
|
||||||
|
性别: |
男女均可 |
Gender: |
Both |
||||||
|
随机方法(请说明由何人用什么方法产生随机序列): |
本研究由非研究参与人员采用计算机网络实现随机化,按1:1随机分为2组 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
Eligible patients will be allocated according to a web-based randomization service using a 1:1 ratio. |
||||||||
|
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 |
|
盲法: |
未说明 |
|
Blinding: |
Not stated |
|
试验完成后的统计结果(上传文件): |
|
|
Calculated Results after
|
|
|
是否共享原始数据: IPD sharing |
是Yes |
|
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): |
ResMan 平台, http://www.medresman.org |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
http://www.medresman.org |
|
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: |
ResMan |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
ResMan |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |