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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2400092516 |
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最近更新日期: Date of Last Refreshed on: |
2024-11-18 17:08:31 |
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注册时间: Date of Registration: |
2024-11-18 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: |
在慢性心衰人群中探索超短心率变异性和房颤的关系 |
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Public title: |
To explore the association between ultra-short heart rate variability and atrial fibrillation in chronic heart failure population |
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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: |
在慢性心衰人群中探索超短心率变异性和房颤的关系 |
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Scientific title: |
To explore the association between ultra-short heart rate variability and atrial fibrillation in chronic heart failure population |
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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: |
唐晓笛 |
研究负责人: |
何榕 |
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Applicant: |
Xiaodi Tang |
Study leader: |
Rong He |
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申请注册联系人电话: Applicant telephone: |
+86 182 1105 5183 |
研究负责人电话: Study leader's telephone: |
+86 131 4109 4403 |
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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: |
867817181@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
dr_herong@sina.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
无 |
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: |
北京市昌平区立汤路168号 |
研究负责人通讯地址: |
北京市昌平区立汤路168号 |
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Applicant address: |
168 Litang Road, Changping District, Beijing, China |
Study leader's address: |
168 Litang Road, Changping District, Beijing, China |
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申请注册联系人邮政编码: Applicant postcode: |
102218 |
研究负责人邮政编码: Study leader's postcode: |
102218 |
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申请人所在单位: |
北京清华长庚医院 |
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Applicant's institution: |
Beijing Tsinghua Changgung Hospital |
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研究负责人所在单位: |
北京清华长庚医院 |
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Affiliation of the Leader: |
Beijing Tsinghua Changgung Hospital |
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是否获伦理委员会批准: |
是/Yes |
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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: |
24674-4-01 |
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: |
北京清华长庚医院医学伦理委员会 |
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Name of the ethic committee: |
Beijing Tsinghua Changgeng Hospital Medical Ethics Committe |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-11-14 00:00:00 |
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伦理委员会联系人: |
刘曼婷 |
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Contact Name of the ethic committee: |
Manting Liu |
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伦理委员会联系地址: |
北京市昌平区立汤路168号 |
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Contact Address of the ethic committee: |
China 168 Litang Road, Changping District, Beijing, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 56118567 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
IRB@btch.edu.cn |
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研究实施负责(组长)单位: |
北京清华长庚医院 |
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Primary sponsor: |
Beijing Tsinghua Changgung Hospital |
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研究实施负责(组长)单位地址: |
北京市昌平区立汤路168号 |
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Primary sponsor's address: |
China 168 Litang Road, Changping District, Beijing, China |
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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: |
本研究为观察性研究,无经费 |
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Source(s) of funding: |
The study was observational and had no funding |
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Target disease: |
Chronic heart failure |
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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: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
本研究的主要目的是在心衰这一房颤高发人群中,观察usHRV和AF发生风险的关系,探索自主神经在心衰人群中导致房颤及其他不良事件中发挥的作用。 |
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Objectives of Study: |
The main objective of this study was to observe the relationship between usHRV and AF risk in heart failure, a population with a high incidence of atrial fibrillation, and to explore the role of autonomic nerve in atrial fibrillation and other adverse events in people with heart failure. |
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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: |
年龄≥18岁。 符合《2024年中国心力衰竭诊断和治疗指南》心衰诊断标准的射血分数轻度下降、下降和射血分数改善的慢性心衰人群。满足以下条件: 1.病史:冠状动脉粥样硬化性心脏病、高血压病、心力衰竭高危因素,使用利尿剂,端坐呼吸/夜间阵发性呼吸困难 2.体征:肺部啰音、双下肢水肿、心脏杂音、颈静脉充盈、心尖搏动侧移或弥散 3.胸部X线片提示肺淤血/水肿和心脏增大、心电图异常 4.NT-proBNP≥125ng/L或BNP≥35ng/L,或强烈怀疑为心力衰竭或NT-proBNP/BNP不可用 5.超声心动图提示LVEF<50% NYHA分级II-III级 |
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Inclusion criteria |
Age ≥18 years. People with chronic heart failure who meet the criteria for the diagnosis and Treatment of heart failure in the 2024 Chinese Guidelines for the Diagnosis and Treatment of Heart Failure with mild decline in ejection fraction, decrease in ejection fraction, or improvement in ejection fraction. Meet the following conditions: 1. Medical history: high risk factors for coronary atherosclerotic heart disease, hypertension and heart failure, use of diuretics, upright breathing/nocturnal paroxysmal dyspnea 2. Signs: lung rales, edema of both lower limbs, heart murmurs, filling of the jugular vein, lateral or diffuse apex beats 3. Chest X-ray shows pulmonary congestion/edema, heart enlargement and abnormal electrocardiogram 4.NT-proBNP≥125ng/L or BNP≥35ng/L, or strongly suspected heart failure or NT-proBNP/BNP unavailable 5. Echocardiography indicated LVEF < 50% NYHA Grade II to III |
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排除标准: |
既往明确诊断为心房颤动、心房扑动的人群 心房起搏依赖的患者 急性心衰及慢性心衰急性发作的患者 严重肝肾疾患(eGFR<30 mL/min/1.73m2)、严重肺部疾病、恶性肿瘤及精神疾病病史; 妊娠妇女、计划在研究期间妊娠或研究期间无法做到有效避孕的育龄妇女 疾病导致预期寿命<12月; 未签署知情同意书。 |
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Exclusion criteria: |
People who have previously been diagnosed with atrial fibrillation or atrial flutter Patients with atrial pacing dependence Patients with acute heart failure and acute episodes of chronic heart failure History of severe liver and kidney diseases (eGFR < 30 mL/min/1.73m2), severe lung diseases, malignant tumors, and mental illness; Pregnant women, women of childbearing age who plan to become pregnant during the study period, or who are unable to use effective contraception during the study period Life expectancy due to disease < 12 months; No informed consent is signed. |
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研究实施时间: Study execute time: |
从 From 2024-11-20 00:00:00至 To 2026-02-28 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 |
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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: |
尚未开始 Not yet 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 |
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: |
CRF;EDC |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF;EDC |
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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 |