Acute Coronary Syndrome
Conditions
Interventions
None listed
Sponsors
Fujita Health University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients admitted to Fujita Health University Hospital with acute coronary syndromes who underwent PCI or who were judged not to require invasive treatment. Patients who have given their free and voluntary written consent to participate in this study after receiving full explanation and with full understanding. Patients 20 years of age or older at the time consent is obtained
Exclusion criteria
Exclusion criteria: 1. Cases of acute coronary syndrome in which the lesion responsible for this acute coronary syndrome did not undergo the necessary revascularization procedures and remained as an obstructive lesion. 2. Cases after coronary artery bypass grafting 3. Cases in which CT imaging is not possible due to allergy to contrast agent 4. Cases with estimated glomerular filtration rate (eGFR) <30 5. Cases with pregnant or lactating women 6. Patients deemed by the attending physician to be unsuitable for participation in the study (including issues with imaging conditions) 7. Patients deemed inappropriate by the Principal Investigator or Principal Investigator for other reasons
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Plaque extension on coronary CT one year after the onset of acute coronary syndrome compared to immediately after the onset of acute coronary syndrome. | — |
Secondary
| Measure | Time frame |
|---|---|
| Cardiovascular events: all-cause mortality, cardiac death, acute coronary syndrome, angina requiring hospitalization, heart failure requiring hospitalization CT findings: changes in non-calcified plaque volume and pericardial fat in plaque quantitative evaluation Rehabilitation indices: change in cardiac anaerobic metabolic threshold (AT), maximal oxygen uptake (peak VO2), and muscle mass | — |
Countries
Japan
Contacts
Public ContactHideki Kawai
Fujita Health University Department of Cardiology
Outcome results
None listed