|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2400087110 |
|
最近更新日期: Date of Last Refreshed on: |
2024-07-19 16:44:55 |
|
注册时间: Date of Registration: |
2024-07-19 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
心脏再同步治疗患者的数字化临床管理的随机对照研究 |
|
Public title: |
A randomized controlled study of digital clinical management of Cardiac resynchronization therapy patients |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
数字化临床管理系统对接受心脏再同步治疗治疗的慢性心力衰竭患者临床预后的影响及评价 |
|
Scientific title: |
Effect and evaluation of digital clinical management system on clinical prognosis of chronic heart failure patients receiving Cardiac resynchronization therapy treatment |
|
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: |
孙卫平 |
研究负责人: |
孙卫平 |
|
Applicant: |
Weiping Sun |
Study leader: |
Weiping Sun |
|
申请注册联系人电话: Applicant telephone: |
+86 186 1131 2085 |
研究负责人电话:
Study leader's |
+86 186 1131 2085 |
|
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: |
18611312085@163.com |
研究负责人电子邮件: Study leader's E-mail: |
18611312085@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: |
北京市朝阳区安贞路2号 |
研究负责人通讯地址: |
北京市朝阳区安贞路2号 |
|
Applicant address: |
2 Anzhen Road, Chaoyang District, Beijing |
Study leader's address: |
2 Anzhen Road, Chaoyang District, Beijing |
|
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: |
首都医科大学附属北京安贞医院 |
||
|
Applicant's institution: |
Beijing Anzhen Hospital affiliated to Capital Medical University |
||
|
研究负责人所在单位: |
首都医科大学附属北京安贞医院 |
||
|
Affiliation of the Leader: |
Beijing Anzhen Hospital affiliated to Capital Medical 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: |
KS2023080 |
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: |
首都医科大学附属北京安贞医院伦理委员会 |
||
|
Name of the ethic committee: |
Ethics Committee of Beijing Anzhen Hospital affiliated to Capital Medical University |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2024-01-05 00:00:00 | ||
|
伦理委员会联系人: |
吴朝阳 |
||
|
Contact Name of the ethic committee: |
Zhaoyang Wu |
||
|
伦理委员会联系地址: |
北京市朝阳区安贞路2号 |
||
|
Contact Address of the ethic committee: |
2 Anzhen Road, Chaoyang District, Beijing |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 158 1122 1587 |
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: |
首都医科大学附属北京安贞医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Beijing Anzhen Hospital affiliated to Capital Medical University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
北京市朝阳区安贞路2号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
2 Anzhen Road, Chaoyang District, Beijing |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
自筹 |
||||||||||||||||||||||
|
Source(s) of funding: |
self-funding |
||||||||||||||||||||||
|
研究疾病: |
慢性心力衰竭 |
||||||||||||||||||||||
|
Target disease: |
Chronic heart failure |
||||||||||||||||||||||
|
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: |
探索性研究/预试验 | ||||||||||||||||||||||
|
Study phase: |
0 |
||||||||||||||||||||||
|
研究设计: |
随机平行对照 |
||||||||||||||||||||||
|
Study design: |
Parallel |
||||||||||||||||||||||
|
研究目的: |
本临床研究针对符合CRT指征并行CRT治疗的心衰患者,初步探索数字化临床管理系统的有效性,以有效控制患者危险因素、提高患者带病生活质量及患者临床预后。 |
||||||||||||||||||||||
|
Objectives of Study: |
In this clinical study, the effectiveness of digital clinical management system was initially explored for patients with heart failure who met CRT indications and were treated with CRT, so as to effectively control patients' risk factors, improve patients' quality of life and clinical prognosis. |
||||||||||||||||||||||
|
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: 符合 2021 年欧洲心脏病学会发布的最新版慢性心力衰竭诊断与治疗指南中 CRT 装置的植入指征,并接受手术治疗 2: 年龄40-65周岁,男女不限 3: 自愿签署知情同意书 |
||||||||||||||||||||||
|
Inclusion criteria |
1: Meet the indications for implantation of CRT devices in the latest edition of the European Society of Cardiology Guidelines for the Diagnosis and Treatment of Chronic heart Failure published in 2021, and receive surgical treatment 2: Age 40-65 years old, male or female 3: Voluntarily sign informed consent |
||||||||||||||||||||||
|
排除标准: |
1: 术后起搏装置工作异常者,或出现突发恶性心律失常等严重并发症者; 2: 存在认知功能障碍或严重精神疾病等 3: 合并恶性肿瘤或严重肝、肾、肺部疾病等 4: 原发性心脏瓣膜疾病 5: 吸毒者或恶病质患者 6: 最近3个月内的急性心肌梗塞或冠脉搭桥 7: 近1年参加其它药物临床试验者 |
||||||||||||||||||||||
|
Exclusion criteria: |
1: Patients with abnormal operation of pacing device or severe complications such as sudden malignant arrhythmia 2: Cognitive dysfunction or severe mental illness 3: Complicated with malignant tumor or serious liver, kidney, lung disease 4: Primary heart valve disease 5: Drug addicts or patients with cachexia 6: Acute myocardial infarction or coronary artery bypass within the last 3 months 7: Participants in clinical trials of other drugs in the last 1 year |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2024-07-20 00:00:00至 To 2026-07-20 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-07-20 00:00:00 至 To 2026-07-20 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): |
交互式网络响应系统 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
interactive web response system,IWRS |
||||||||
|
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: |
无 |
|
Blinding: |
none |
|
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): |
研究结束后半年公开在ResMan系统 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Half a year after the completion of the research, it will be publicly available on the ResMan |
|
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: |
数据采集和管理由两部分组成,一部分为病历记录表,另一部分为哈瑞特电子采集与管理系统,并由临床研究协调员指导完成 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Data collection and management consists of two parts, one is the medical record form, the other is the Harriet electronic collection and management system, and is guided by the clinical research coordinator |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |