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临床试验/NCT07038083
NCT07038083招募中不适用

REal-world Data of CARdiometabolic ProtEcTion

Sun Yat-sen University1 个研究点 分布在 1 个国家目标入组 40,000 人开始时间: 2014年1月1日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
40,000
试验地点
1
主要终点
all-cause mortality

研究概览

简要总结

This study is a single-center, historical prospective cohort study including patients diagnosed with metabolic cardiovascular disease, including hypertension, diabetes, obesity, dyslipidemia, hyperuricemia. The primary outcome of the study is all-cause death and cardiovascular death, and the secondary outcome is major adverse cardiovascular events. We aim to measure associations of established or suspected cardiometabolic disease (CMD) risk factors and cardiovascular disease outcomes in a real-world representative cohort.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients over 18 years old;
  • Patients with clinical diagnosis of metabolic cardiovascular disease, including hypertension, diabetes, obesity, dyslipidemia, hyperuricemia.
  • Hypertension and normal high blood pressure: Three standardized blood pressure measurements in the clinic on different days, and all the blood pressure values of the three measurements were systolic blood pressure ≥ 120 mmHg and/or diastolic blood pressure ≥ 80 mmHg;
  • Diabetes: ① Typical symptoms of diabetes, and any of the following: ② Random blood glucose ≥ 11.1 mmol/L; ③ Fasting blood glucose (FPG) ≥ 7.0 mmol/L; ④ OGTT 2-hour postprandial blood glucose ≥ 11.1 mmol/L; ⑤ HbA1c ≥ 6.5%;
  • Obesity and overweight: Body mass index (BMI) ≥ 24 kg/m²;
  • Dyslipidemia: At least one of the following lipid indicators is abnormal: ① Total cholesterol (TC) ≥ 6.2 mmol/L; ② Low-density lipoprotein cholesterol (LDL-C) ≥ 4.1 mmol/L; ③ High-density lipoprotein cholesterol (HDL-C) < 1.0 mmol/L; ④ Triglyceride (TG) ≥ 2.3 mmol/L; ⑤ Lipoprotein(a) ≥ 30 mg/dL;
  • Hyperuricemia: The fasting blood uric acid levels on two different days were > 420 μmol/L (7 mg/dL) in men and > 360 μmol/L (6 mg/dL) in women.

排除标准

  • Patients unable to provide informed consent.

结局指标

主要结局

all-cause mortality

时间窗: Through study completion, an average of 5 years

Death due to any cause after enrollment

Cardiovascular death

时间窗: Through study completion, an average of 5 years

Death caused by cardiac causes

次要结局

  • Major adverse cardiovascular events(Through study completion, an average of 5 years)

研究者

发起方
Sun Yat-sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Xiao-dong Zhuang

Professor

Sun Yat-sen University

研究点 (1)

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