Clinical Trial

A Study on the Peripheral Blood in Patients With Acute Coronary Syndrome

Recruiting
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Record status
This record was last updated July 25, 2025 (before its estimated August 2025 completion). Its status may not reflect the trial's current state.
Summary
The goal of this study is to conduct analyses the changes of cell growth factors, inflammatory factors, metabolites, plasma proteome, etc. in the blood of patients with ACS (acute coronary syndrome), as well as their correlations with the disease prognosis, based on multi-omics or other related research methods. The main questions it aims to answer are: The growth factors that have significant changes in the peripheral blood of the ACS population, especially fibroblast growth factors? Inflammatory factors and chemokines related to the onset of ACS? The metabolites and proteins that are significantly altered in the peripheral blood after the onset of ACS? Researchers will compare ACS population to CCS (Chronic Coronary Syndrome) population, and control group (patients without coronary artery stenosis, valvular heart disease, structural heart disease, or any other kind of cardiomyopathy).The peripheral venous blood from the participants will be collected within 24 hours after their admission to the hospital.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-04-24; most recent amendment 2025-07-21.
Trial Details
NCT Number NCT06955143
Lead Sponsor Second Affiliated Hospital of Wenzhou Medical University
Collaborators: The Central Hospital of Lishui City
Conditions Acute Coronary Syndrome, Chronic Coronary Syndrome
Enrollment 310 participants
Start Date 2025-03-11
Primary Completion 2025-08 (estimated)
Study Completion 2025-12 (estimated)
Updated on ClinicalTrials.gov 2025-07-25