|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2400092594 |
|
最近更新日期: Date of Last Refreshed on: |
2024-11-19 17:01:11 |
|
注册时间: Date of Registration: |
2024-11-19 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
阿托伐他汀联合海博麦布治疗高脂血症的安全性监测:一项多中心、医院集中监测研究 |
|
Public title: |
Safety monitoring of atorvastatin combined with hybomib in the treatment of hyperlipidemia: a multicentre, hospital-focused monitoring study |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
阿托伐他汀联合海博麦布治疗高脂血症的安全性监测:一项多中心、医院集中监测研究 |
|
Scientific title: |
Safety monitoring of atorvastatin combined with hybomib in the treatment of hyperlipidemia: a multicentre, hospital-focused monitoring study |
|
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: |
段蓉 |
研究负责人: |
李正翔 |
|
Applicant: |
Duan Rong |
Study leader: |
Li Zhengxiang |
|
申请注册联系人电话: Applicant telephone: |
+86 137 5206 0959 |
研究负责人电话:
Study leader's |
+86 138 2089 3896 |
|
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: |
duanrong2001@163.com |
研究负责人电子邮件: Study leader's E-mail: |
13820893896@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: |
中国天津市和平区鞍山道154号 |
研究负责人通讯地址: |
中国天津市和平区鞍山道154号 |
|
Applicant address: |
154 Anshan Road, Heping District, Tianjin, China |
Study leader's address: |
154 Anshan Road, Heping District, Tianjin, 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: |
天津医科大学总医院 |
||
|
Applicant's institution: |
Tianjin Medical University General Hospital |
||
|
研究负责人所在单位: |
天津医科大学总医院 |
||
|
Affiliation of the Leader: |
Tianjin Medical University General Hospital |
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
IRB2024-YX-476-01 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
|
批准本研究的伦理委员会名称: |
天津医科大学总医院医学伦理委员会 |
||
|
Name of the ethic committee: |
Medical Ethics Committee of Tianjin Medical University General Hospital |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2024-10-31 00:00:00 | ||
|
伦理委员会联系人: |
金冬来 |
||
|
Contact Name of the ethic committee: |
Jin Donglai |
||
|
伦理委员会联系地址: |
中国天津市和平区鞍山道154号 |
||
|
Contact Address of the ethic committee: |
154 Anshan Road, Heping District, Tianjin, China |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 22 6036 1044 |
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: |
天津医科大学总医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Tianjin Medical University General Hospital |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
中国天津市和平区鞍山道154号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
154 Anshan Road, Heping District, Tianjin, China |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
北京科创医学发展基金会 |
||||||||||||||||||||||
|
Source(s) of funding: |
Beijing Science and Technology Innovation Medical Development Foundation |
||||||||||||||||||||||
|
研究疾病: |
高脂血症 |
||||||||||||||||||||||
|
Target disease: |
Hyperlipidemia |
||||||||||||||||||||||
|
研究疾病代码: |
|
||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||
|
研究类型: |
观察性研究 |
||||||||||||||||||||||
|
Study type: |
Observational study |
||||||||||||||||||||||
|
研究所处阶段: |
上市后药物 | ||||||||||||||||||||||
|
Study phase: |
4 |
||||||||||||||||||||||
|
研究设计: |
横断面 |
||||||||||||||||||||||
|
Study design: |
Cross-sectional |
||||||||||||||||||||||
|
研究目的: |
主要研究目的: 评估阿托伐他汀联合海博麦布治疗高脂血症的不良反应发生的类型、临床表现和发生率 次要研究目的: 1.探索阿托伐他汀联合海博麦布治疗高脂血症的各类不良反应的严重程度、预后及转归 2. 研究阿托伐他汀联合海博麦布治疗高脂血症不良反应发生的主要影响因素 |
||||||||||||||||||||||
|
Objectives of Study: |
Main research objectives: To evaluate the types, clinical manifestations and incidence of adverse reactions of atorvastatin combined with hybomib in the treatment of hyperlipidemia Secondary research objectives: 1. To explore the severity, prognosis and outcome of various adverse reactions of atorvastatin combined with hybomib in the treatment of hyperlipidemia 2. To study the main influencing factors of the adverse reactions of atorvastatin combined with hybomib in the treatment of hyperlipidemia |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
1. 明确高脂血症诊断 2. 接受阿托伐他汀联合海博麦布治疗的患者 3. 患者性别、年龄、基础疾病均不限 4. 用药时长、药品品规、合并用药情况均不限 |
||||||||||||||||||||||
|
Inclusion criteria |
1. Confirm the diagnosis of hyperlipidemia 2. Patients receiving atorvastatin combined with hybomaib 3. The patient's gender, age and underlying disease are not limited 4. Duration of drug use, drug specifications, and combination of drugs are not limited |
||||||||||||||||||||||
|
排除标准: |
无法采集本项研究所需要信息的患者 |
||||||||||||||||||||||
|
Exclusion criteria: |
Patients whose information was not available for this study |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2024-11-01 00:00:00至 To 2025-06-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-11-20 00:00:00 至 To 2025-02-28 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): |
无 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
||||||||
|
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: |
|
|
Blinding: |
|
|
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 |
否No |
|
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): |
不共享 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None |
|
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: |
本研究采用 EDC(Electronic Data CaptureSystem,电子数据获取系统)同步录入。网址登录时的用户名和密码由研究负责单位统一进行分配,各监测医院进行EDC数据的录入,各监测医院质量控制员进行数据的审查和纠错,控制数据录入质量。研究负责单位数据管理员对全部数据进行统一审核,发现问题及时与各监测医院数据管理员沟通并解决。所有数据经检查无错误后提取建立可用于统计分析的数据库。 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
In this study, EDC (Electronic Data CaptureSystem, electronic data acquisition System) was used for synchronous input. The user name and password of the website login are uniformly assigned by the research unit in charge, EDC data entry is carried out in each monitoring hospital, and the quality controller of each monitoring hospital reviews and corrects the data to control the quality of data entry. The data administrator of the research unit shall conduct a unified audit of all data, and communicate with the data administrator of each monitoring hospital in time to solve any problems found. All the data are checked for error and extracted to build a database that can be used for statistical analysis. |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |