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注册号: Registration number: |
ChiCTR2400080900 |
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最近更新日期: Date of Last Refreshed on: |
2024-02-18 08:56:47 |
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注册时间: Date of Registration: |
2024-02-18 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: |
急性Standard B型主动脉夹层腔内支架修复术后健康相关生活质量研究 |
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Public title: |
Health-related quality of life of patients with acute Standford B aortic dissection who underwent thoracic aortic repair |
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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: |
急性Standard B型主动脉夹层腔内支架修复术后健康相关生活质量研究 |
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Scientific title: |
Health-related quality of life of patients with acute Standford B aortic dissection who underwent thoracic aortic repair |
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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: |
郭宝磊 |
研究负责人: |
符伟国 |
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Applicant: |
Baolei Guo |
Study leader: |
Weiguo Fu |
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申请注册联系人电话: Applicant telephone: |
+86 135 6424 0966 |
研究负责人电话:
Study leader's |
+86 138 0176 0929 |
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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: |
guo.baolei@zs-hospital.sh.cn |
研究负责人电子邮件: Study leader's E-mail: |
fu.weiguo@zs-hospital.sh.cn |
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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, 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, 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: |
B2024-003R |
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医学伦理委员会 |
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Name of the ethic committee: |
Medical 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: |
2024-01-29 00:00:00 | ||
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伦理委员会联系人: |
杨梦婕 |
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Contact Name of the ethic committee: |
Mengjie Yang |
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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 21 3158 7871 |
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, 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号复旦大学附属中山医院 |
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Primary sponsor's address: |
180 Fenglin Road, Xuhui District, Shanghai City |
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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: |
复旦大学附属中山医院临床研究专项基金 |
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Source(s) of funding: |
Clinical Research Funding of Zhongshan Hospital of Fudan University |
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研究疾病: |
急性Standard B型主动脉夹层 |
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Target disease: |
Acute Standford B aortic dissection |
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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: |
回顾性研究 | ||||||||||||||||||||||
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Study phase: |
Retrospective study |
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研究设计: |
横断面 |
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Study design: |
Cross-sectional |
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研究目的: |
评价急性Standard B型主动脉夹层腔内支架修复术后患者的短期及长期健康相关生命质量及其影响因素,并与中国一般人群的HRQOL常模数据进行比对,探索性别、治疗策略和年龄等因素对TEVAR术后患者HRQoL的影响。 |
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Objectives of Study: |
To evaluate the short - and long-term health-related quality of life and its influencing factors of patients after acute Standard B type aortic dissection and stent repair, and to compare with the HRQOL constant modulus data of the Chinese general population to explore the effects of gender, treatment strategy and age on HRQoL of patients after TEVAR. |
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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.慢性Standard B型主动脉夹层患者; 2.既往有主动脉置换或TEVAR病史的夹层患者; 3.患者不能(如死亡或无法配合完成调查)或不愿意参与本研究的; 研究者判断患者不适合(如患有其他严重健康问题或心理健康状态不佳)参与本试验的。 |
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Exclusion criteria: |
1. Patients with chronic Standard B aortic dissection; 2. Dissection patients with a history of aortic replacement or TEVAR; 3. The patient is unable (such as death or unable to cooperate with the investigation) or unwilling to participate in the study; Patients judged by the investigator to be unfit (such as those with other serious health problems or poor mental health) to participate in the trial. |
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研究实施时间: Study execute time: |
从 From 2024-01-29 00:00:00至 To 2024-10-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-02-29 00:00:00 至 To 2024-04-30 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): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
none |
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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 |
否No |
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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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
none |
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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: |
通过复旦大学附属中山医院血管外科医疗数据库寻找符合条件的患者,并进行验证。通过电话访谈收集每位参与者的健康相关生活质量信息。患者需要填写一份包含社会人口学信息、SF-36量表和EQ-5D-5L量表相关数据的结构化问卷。由两人配合录入至数据库中,一人读取数据,一人电脑录入,双人同时审核的方法进行。研究者必须妥善处理所有临床研究过程中获得 的数据,以保证参与临床研究的受试者的权利。在所有的疑问表返回后,将对数 据进行最后的修改。对于所有的修改及更新都需要进行记录及归档。在数据完全核实后,召开数据管理会议,对关键数据的修改及更新情况进行总结。由数据管理人员宣布数据的锁定并保存密码。数据锁定后,统计分析计划将不再更改。数据将被转到统计人员供统计分析使用。数据库锁定后的数据可以进行分析和撰写 文章。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Qualified patients were searched for and verified through the vascular surgery medical database of Zhongshan Hospital Affiliated to Fudan University. Health-related quality of life information was collected for each participant through telephone interviews. Patients were asked to complete a structured questionnaire that included sociodemographic information and data on the SF-36 and EQ-5D-5L scales. Two people cooperate to enter into the database, one person reads the data, one person enters the computer, and two people review at the same time. All data obtained during clinical studies must be properly handled by the investigator to ensure the rights of participants in the clinical study. After all query tables are returned, a final modification of the data is made. All changes and updates need to be recorded and filed. After the data is completely verified, a data management meeting is held to summarize the modification and update of key data. The data manager announces the locking of the data and saves the password. After the data is locked, the statistical analysis plan is not changed. The data will be passed on to statisticians for statistical analysis. The data locked in the database can be analyzed and written. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |