跳至主要内容
临床试验/NCT06880575
NCT06880575招募中不适用

Seniors Integrated Longitudinal CardioVascular Evaluation of Coronary Heart Disease: a Multicenter, Prospective Registry in China (SILVER-China)

Beijing Hospital1 个研究点 分布在 1 个国家目标入组 10,139 人开始时间: 2024年11月6日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
10,139
试验地点
1
主要终点
major adverse cardiovascular events

研究概览

简要总结

This study aims to establish a nationwide cohort and biobank of elderly patients with coronary heart disease (CHD) and to develop risk prediction models and clinical treatment optimization plans based on this data. The specific research content is as follows:

The Study plan to continuously enroll hospitalized elderly CHD patients across 50 centers nationwide. Using networked electronic data collection technology, standardized methods and protocols will be used to gather demographic information (such as age, gender, education level, income, etc.), clinical information (medical history, past treatment records, current treatment plans, surgical records, medication use, etc.), lifestyle information (dietary habits, exercise frequency, smoking, drinking, etc.), biological information (such as inflammatory markers, etc.), and physical examination data (such as blood pressure, ECG, sleep monitoring, imaging examinations, etc.). These patients will be followed up long-term (1 month, 6 months, 1 year, and annually thereafter for up to 5 years) to establish a database that meets international standards. Centers meeting the criteria will also retain biological samples, creating a multicenter biobank for elderly CHD patients.

Second, based on the established clinical cohort, a risk prediction model for elderly CHD patients will be developed, including mortality risk, ischemic risk, bleeding risk, etc. Additionally, optimized clinical diagnostic and treatment plans will be formulated to improve the treatment outcomes and quality of life for elderly CHD patients. This research is expected to provide scientific evidence and technical support for the prevention, diagnosis, and treatment of CHD in elderly patients.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
75 Years 至 —(Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •① Age requirements: Participants are ≥ 75 years old;
  • •This time he was admitted to the hospital due to angina pectoris and other coronary heart disease-related symptoms
  • •③ Conform to the diagnosis of coronary heart disease: meet any one of the following conditions:
  • •This admission was performed for coronary angiography, coronary artery CTA confirmed coronary heart disease;
  • •Previous clear coronary angiography, coronary artery Coronary heart disease diagnosed by imaging evidence such as CTA evidence;
  • •The attending physician according to the patient's symptoms, medical history, myocardial injury markers, electrocardiogram, echo cardiography, myocardial radionuclide imaging, etc. diagnosed coronary heart disease.
  • •④ Informed consent: Participants must be able to understand the content of the study, voluntarily participate in the study, and sign the informed consent form.

排除标准

  • •Combined with severe non-cardiovascular disease: life expectancy does not exceed 6 months, such as advanced cancer or other end-stage disease;
  • •Unable to cooperate with long-term follow-up: such as patients with severe cognitive impairment or severe mental illness; ③ Non-cardiogenic death within 24 hours after admission.

结局指标

主要结局

major adverse cardiovascular events

时间窗: From enrollment to the end of follow up at 5 years

MACCE, refers to the composite endpoint including all-cause mortality, non-fatal myocardial infarction, non-fatal stroke, and ischemia-driven revascularization

次要结局

  • all-cause mortality(From enrollment to the end of follow up at 5 years)
  • non-fatal stroke and ischemia-driven revascularization(From enrollment to the end of follow up at 5 years)
  • cardiogenic death(From enrollment to the end of follow up at 5 years)
  • non-fatal myocardial infarction(From enrollment to the end of follow up at 5 years)
  • stent thrombosis(From enrollment to the end of follow up at 5 years)
  • major bleeding(From enrollment to the end of follow up at 5 years)
  • all BARC bleeding(From enrollment to the end of follow up at 5 years)
  • NACE(From enrollment to the end of follow up at 5 years)
  • Quality of life(From enrollment to the end of follow up at 5 years)
  • angina pectoris readmission(From enrollment to the end of follow up at 5 years)
  • heart failure(From enrollment to the end of follow up at 5 years)

研究者

发起方
Beijing Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Fusui Ji, MD

Chief physician and dean of Beijing Hospital

Beijing Hospital

研究点 (1)

Loading locations...

相似试验