Clinical Trials Directory

Trials / Completed

CompletedNCT04797819

Serum Soluble ST2 and Plaque Vulnerability in Patients With Acute Coronary Syndrome

Elevated Serum Soluble ST2 Level is Associated With Increased Plaque Vulnerability in Patients With Non-ST Elevation Acute Coronary Syndrome

Status
Completed
Phase
Study type
Observational
Enrollment
120 (actual)
Sponsor
RenJi Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers

Summary

This study aimed to assess the association between serum sST2 level and plaque vulnerability in ACS patients. It is hypothesized that serum sST2 level may be related to plaque components and closely associated with plaque vulnerability.

Detailed description

Serum soluble suppression of tumorigenicity-2 (sST2) has emerged as a novel biomarker of atherosclerotic disease. This study aimed to investigate whether elevated serum sST2 level is related to coronary plaque components detected on coronary computed tomography angiography (CCTA) and plaque vulnerability in non-ST elevation acute coronary syndromes (ACS) patients. 167 lesions in 120 non-ST elevation ACS patients were prospectively enrolled and evaluated by CCTA in this study. Blood were taken from antecubital vein during patient's hospitalization for angiography. Serum sST2 level was measured by commerical ELISA kits (Presage ST2 Assay Kit, Critical Diagnostics). CCTA were performed using a 320-slice CT scanner (Aquilion ONE, Toshiba Medical Systems, Otawara, Japan). Coronary plaque components were analyzed cross each of the lesions using commercialized software package (QAngio CT, Medis, The Netherlands).

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTCoronary plaque componentsCoronary plaque components were detected by CCTA method

Timeline

Start date
2019-01-01
Primary completion
2019-12-31
Completion
2019-12-31
First posted
2021-03-15
Last updated
2021-03-24

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04797819. Inclusion in this directory is not an endorsement.