|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2400088128 |
|
最近更新日期: Date of Last Refreshed on: |
2024-08-13 10:29:19 |
|
注册时间: Date of Registration: |
2024-08-12 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
SGLT2i治疗前后HFrEF合并/不合并房颤患者EAT 影像组学特征和肠道菌群及其代谢产物变化及其与患者临床特征之间关系的研究 |
|
Public title: |
Study on the relationship between EAT imaging omics characteristics, changes in gut microbiota and metabolites, and clinical features of HFrEF patients with and without atrial fibrillation before and after SGLT2i treatment |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
SGLT2i治疗前后HFrEF合并/不合并房颤患者EAT 影像组学特征和肠道菌群及其代谢产物变化及其与患者临床特征之间关系的研究 |
|
Scientific title: |
Study on the relationship between EAT imaging omics characteristics, changes in gut microbiota and metabolites, and clinical features of HFrEF patients with and without atrial fibrillation before and after SGLT2i 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: |
马玉兰 |
研究负责人: |
马玉兰 |
|
Applicant: |
Yu-Lan Ma |
Study leader: |
Yu-Lan Ma |
|
申请注册联系人电话: Applicant telephone: |
+86 183 9711 9989 |
研究负责人电话:
Study leader's |
+86 183 9711 9989 |
|
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: |
mylfamai@163.com |
研究负责人电子邮件: Study leader's E-mail: |
mylfamai@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: |
青海省西宁市城西区同仁路29号 |
研究负责人通讯地址: |
青海省西宁市城西区同仁路29号 |
|
Applicant address: |
29 Tongren Road, Chengxi, Xining, Qinghai |
Study leader's address: |
29 Tongren Road, Chengxi, Xining, Qinghai |
|
申请注册联系人邮政编码: Applicant postcode: |
810000 |
研究负责人邮政编码: Study leader's postcode: |
810000 |
|
申请人所在单位: |
青海省心脑血管专科医院 |
||
|
Applicant's institution: |
Qinghai Cardio-Cerebrovascular Specialty Hospital/Qinghai High Altitude Medical Research Institute |
||
|
研究负责人所在单位: |
青海省心脑血管专科医院 |
||
|
Affiliation of the Leader: |
Qinghai Cardio-Cerebrovascular Specialty Hospital/Qinghai High Altitude Medical Research Institute |
||
|
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: |
QXYYLL-2024-93 |
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: |
青海省心脑血管专科医院 |
||
|
Name of the ethic committee: |
Qinghai Cardio-Cerebrovascular Specialty Hospital |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2024-08-09 00:00:00 | ||
|
伦理委员会联系人: |
刘楠楠 |
||
|
Contact Name of the ethic committee: |
Liu Nannan |
||
|
伦理委员会联系地址: |
青海省西宁市砖厂路7号 |
||
|
Contact Address of the ethic committee: |
7 Brick Factory Road, Xining, Qinghai |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 139 9720 6546 |
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: |
青海省心脑血管专科医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Qinghai Cardio-Cerebrovascular Specialty Hospital |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
青海省心脑血管专科医院 |
||||||||||||||||||||||
|
Primary sponsor's address: |
Qinghai Cardio-Cerebrovascular Specialty Hospital |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
国家自然科学基金地区科学基金项目 |
||||||||||||||||||||||
|
Source(s) of funding: |
National Natural Science Foundation of China Regional Science Foundation Project |
||||||||||||||||||||||
|
研究疾病: |
心房颤动 |
||||||||||||||||||||||
|
Target disease: |
Atrial fibrillation |
||||||||||||||||||||||
|
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: |
上市后药物 | ||||||||||||||||||||||
|
Study phase: |
4 |
||||||||||||||||||||||
|
研究设计: |
队列研究 |
||||||||||||||||||||||
|
Study design: |
Cohort study |
||||||||||||||||||||||
|
研究目的: |
1. 主要目的:评估SGLT2i对房颤合并HFrEF患者的影响。 2. 次要目的:评估SGLTi对房颤患者心外膜脂肪组织、肠道菌群及其代谢物等相关的影响。 |
||||||||||||||||||||||
|
Objectives of Study: |
1. Primary objective: To evaluate the effect of SGLT2i on atrial fibrillation in Patient with HFrEF. 2. Secondary objectives: To evaluate the effect of SGLT2i on the epicardial adipose tissue volume and gut microbiota. |
||||||||||||||||||||||
|
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)心功能III/IV的HFrEF; (2)HFrEF伴AF患者:所有患者依据既往病史、临床表现及心电图等资料确诊为心房颤动; (3)签署知情同意书; |
||||||||||||||||||||||
|
Inclusion criteria |
(1) HFrEF of heart function III/IV; (2) HFrEF patients with AF: All patients were diagnosed with atrial fibrillation based on past medical history, clinical manifestations, and electrocardiogram data; (3) Sign an informed consent form; |
||||||||||||||||||||||
|
排除标准: |
1.不明原因心肌病、不可控制的心律失常、精神障碍、恶性肿瘤、严重肝肾功能障碍; 2.合并风湿性及其他心脏瓣膜病、人工心脏瓣膜置换术后; 3.严重甲状腺疾病患者; 4.冠脉旁路移植术后或支架植入术后; 5.大量心包积液; 6.肠道功能紊乱; 7.尿路感染者。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1. Unidentified cardiomyopathy, uncontrollable arrhythmia, mental disorders, malignant tumors, and severe liver and kidney dysfunction; 2. After combined rheumatic and other heart valve diseases and artificial heart valve replacement surgery; 3. Patients with severe thyroid diseases; 4. After coronary artery bypass grafting or stent implantation; 5. Massive pericardial effusion; 6. Intestinal dysfunction; 7. Urinary tract infections. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2024-08-09 00:00:00至 To 2027-08-09 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-08-12 00:00:00 至 To 2027-08-09 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): |
前瞻性队列研究 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
Prospective cohort study |
||||||||
|
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 |
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): |
原始数据上传至发表学术刊物指定数据库 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Upload the original data to database of the scientific publication |
|
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: |
本研究采用病例报告表(CRF)模式,在试验启动之前对试验参加人员进行相关培训。 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case report form (CRF) mode was adopted, and participants were trained before the trial started. |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |