|
注册号: Registration number: |
ChiCTR2300071626 |
|
最近更新日期: Date of Last Refreshed on: |
2023-07-20 21:19:47 |
|
注册时间: Date of Registration: |
2023-05-19 00:00:00 |
|
注册号状态: |
补注册 |
|
Registration Status: |
Retrospective registration |
|
注册题目: |
人工生物心脏瓣膜治疗心脏瓣膜疾病在中国人群的真实世界研究 |
|
Public title: |
A real world study of use of bioprosthetic heart valve for heart valve disease treatment in Chinese population |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
人工生物心脏瓣膜治疗心脏瓣膜疾病在中国人群的真实世界研究 |
|
Scientific title: |
A real world study of use of bioprosthetic heart valve for heart valve disease treatment in Chinese population |
|
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: |
张正帅 |
研究负责人: |
刘立明 |
|
Applicant: |
Zhang Zhengshuai |
Study leader: |
Liu Liming |
|
申请注册联系人电话: Applicant telephone: |
+86 185 1904 0869 |
研究负责人电话:
Study leader's |
+86 138 0748 9183 |
|
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: |
zhengshuai.zhang@cardimed.com.cn |
研究负责人电子邮件: Study leader's E-mail: |
liulimingjia@aliyun.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: |
北京市大兴区天富街9号7幢1至3层 |
研究负责人通讯地址: |
湖南省长沙市芙蓉区人民中路139号 |
|
Applicant address: |
Floor 1-3, Building 7, 9 Tianfu Street, Daxing District, Beijing |
Study leader's address: |
139 Renmin Middle Road, Furong District, Changsha, Hu'nan |
|
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: |
北京市普惠生物医学工程有限公司 |
||
|
Applicant's institution: |
Beijing Puhui Biomedical Engineering Co., LTD. |
||
|
研究负责人所在单位: |
中南大学湘雅二医院 |
||
|
Affiliation of the Leader: |
The Second Xiangya Hospital of Central South University |
||
|
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: |
(2022)伦审【临研】第(247)号 |
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: |
中南大学湘雅二医院临床研究伦理委员会 |
||
|
Name of the ethic committee: |
Clinical Research Ethics Committee of the Second Xiangya Hospital, Central South University |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2022-12-14 00:00:00 | ||
|
伦理委员会联系人: |
徐会中 |
||
|
Contact Name of the ethic committee: |
Xu Huizhong |
||
|
伦理委员会联系地址: |
湖南省长沙市芙蓉区人民中路139号医院精卫楼19楼 |
||
|
Contact Address of the ethic committee: |
Floor 9, Jingwei Building, Hospital, 139 Renmin Middle Road, Furong District, Changsha, Hu'nan |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 731 8529 2476 |
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: |
中南大学湘雅二医院 |
||||||||||||||||||||||
|
Primary sponsor: |
The Second Xiangya Hospital of Central South University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
湖南省长沙市芙蓉区人民中路139号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
139 Renmin Middle Road, Furong District, Changsha, Hu'nan |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
江苏释研医药科技有限公司 |
||||||||||||||||||||||
|
Source(s) of funding: |
Jiangsu Shiyan Medical Technology Co., LTD. |
||||||||||||||||||||||
|
研究疾病: |
心脏瓣膜疾病 |
||||||||||||||||||||||
|
Target disease: |
Heart valve disease |
||||||||||||||||||||||
|
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: |
其它 | ||||||||||||||||||||||
|
Study phase: |
N/A |
||||||||||||||||||||||
|
研究设计: |
连续入组 |
||||||||||||||||||||||
|
Study design: |
Sequential |
||||||||||||||||||||||
|
研究目的: |
评估真实世界中,人工生物心脏瓣膜用于心脏瓣膜疾病患者的安全性 |
||||||||||||||||||||||
|
Objectives of Study: |
To evaluate the safety of bioprosthetic heart valves in patients with heart valve disease in the real world. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
根据20家医院登记的心脏瓣膜置换数据,回顾性连续纳入2019年5月至2021年12月31日期间各研究中心首次行人工生物心脏瓣膜置换的心脏瓣膜疾病患者的临床资料,按照纳入、排除标准确定研究对象。针对死亡/失访的患者,尽可能追溯其死亡/失访原因,并进行记录。对于存活患者,采用门诊复查或 电话的方式取得患者同意后,发送电子问卷至患者进行调查。医患两端同步采集数据后进行统计分析,以便获得患者使用生物心脏瓣膜后的中长期生存状态及瓣膜相关并发症情况,总结预后影响因素,对其中长期临床疗效进行评价。 |
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
According to the data of heart valve replacement registered in 20 hospitals, the clinical data of patients with heart valve disease who underwent the first artificial heart valve replacement in each research center from May 2019 to December 31, 2021 were retrospectively included. The study subjects were identified according to the inclusion and exclusion criteria. For the patients who died/lost to follow-up, the causes of death/loss to follow-up were traced back as far as possible and recorded. For the surviving patients, an electronic questionnaire was sent to the patients after obtaining their consent by outpatient review or telephone interview. The data were collected synchronously by doctors and patients for statistical analysis, in order to obtain the medium and long-term survival status and valve-related complications of patients after using biological heart valves, summarize the prognostic factors, and evaluate the medium and long-term clinical efficacy. |
||||||||||||||||||||||
|
纳入标准: |
|||||||||||||||||||||||
|
Inclusion criteria |
|||||||||||||||||||||||
|
排除标准: |
1.经导管瓣膜植入者; 2.曾经或现在有精神类疾病者; 3.严重听力或语言障碍及交流障碍者; 4.研究者认为不适合入组的其他情况者。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1. Transcatheter valve implantation; 2. Patients with past or present mental illness; 3. Severe hearing or language disorders and communication disorders; 4. Other conditions considered by the investigator to be inappropriate for enrollment. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2022-11-01 00:00:00至 To 2024-06-10 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2022-12-15 00:00:00 至 To 2023-12-13 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: |
正在进行 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): |
null |
||||||||
|
是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
不公开/Private |
|
盲法: |
none |
|
Blinding: |
none |
|
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): |
https://edc-cloud.medsci.cn/#/login |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
null |
|
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: |
病例记录表, |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form, CRF |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |