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Exploring the relationship between subclinical atherosclerosis progression and endothelial function - a prospective cohort study

Exploring the relationship between subclinical atherosclerosis progression and endothelial function - a prospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500095684
Enrollment
Unknown
Registered
2025-01-10
Start date
2024-06-11
Completion date
Unknown
Last updated
2025-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

subclinical atherosclerotic diseases

Interventions

Observation group:None

Sponsors

Xuanwu Hospital Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.(1) Combined with at least one cardiovascular disease risk factor, such as hypertension, family history of cardiovascular disease, diabetes, hyperlipidemia, smoking, obesity, etc. 2.(2) Based on routine hospital tests, cardiovascular ultrasound, coronary CTA and other auxiliary examinations, Vascular and endothelial function tests such as brachial-ankle pulse wave velocity (baPWV) and flow-mediated dilation (FMD), Patients diagnosed without definite atherosclerotic disease. 3.(3) Understand the research protocol, voluntarily participate in the study, and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1.(1) Patients with a history of severe atherosclerotic cardiovascular and cerebrovascular events, including a history of old myocardial infarction, acute coronary syndrome, and ischemic/hemorrhagic stroke, as well as patients with suspicious symptoms of transient ischemic attack in the past, who were found to have cardiac embolism or major artery disease. 2.(2) symptomatic peripheral vascular disease, including prior revascularization or amputation; 3.(3) Improve the diagnosis of patients with atherosclerotic diseases after admission tests and examinations; 4.(4) Patients allergic to iodine contrast media; 5.(5) have combined severe liver insufficiency and/or severe renal insufficiency (estimated glomerular filtration rate [eGFR] < 30 ml/min); 6.(6) combined with other infectious diseases, including respiratory system infection, urinary system infection, etc.; 7.(7) Combined with rheumatological and other metabolic diseases, including systemic vasculitis, lupus erythematosus, thyroid dysfunction, etc.; 8.(8) Multiple organ failure and unstable vital signs have been diagnosed with advanced malignant tumors; 9.(9) Pregnant or lactating patients; 10.(10) Suffering from mental illness and unable to cooperate with researchers; 11.(11) Other patients not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Incidence of cardiovascular events (coronary heart disease, myocardial infarction), stroke (hemorrhagic, ischemic), revascularization of any artery, and death (cardiogenic, non-cardiogenic);

Countries

China

Contacts

Public ContactLi jing

Xuanwu Hospital Capital Medical University

shpxbb@sina.com+86 10 8319 8899

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026