Actively Recruiting
Epicardial Cardiac Fat-CT (EPIC-CT)
Led by Instituto Mexicano del Seguro Social · Updated on 2026-01-02
136
Participants Needed
1
Research Sites
60 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Both globally and nationally, heart disease remains the leading cause of death overall and across genders, with ischemic heart disease being the primary cause. It is now understood that multiple risk factors contribute to the development of this condition, notably type 2 diabetes mellitus and obesity, especially an increase in visceral fat. Among these, the role of epicardial fat volume in the presence of atheromatous plaques in patients with coronary artery disease has been emphasized, along with the link between its volume and the risk of ischemic cardiovascular events. Consequently, recent decades have seen focused research on the potential of epicardial fat as a marker for major adverse cardiac events and on strategies to reduce its volume as a treatment goal for patients with risk factors. Selective sodium-glucose cotransporter 2 inhibitors are drugs that, beyond their antihyperglycemic effect, have demonstrated cardiovascular benefits through various mechanisms, including a reduction in epicardial fat. This was supported by a previous study conducted by our research group, although no statistically significant difference was found. On the other hand, GLP-1 agonists are effective drugs for weight control in patients with severe obesity. However, little research has been done on their effect on more localized fat, such as epicardial fat.
CONDITIONS
Official Title
Epicardial Cardiac Fat-CT (EPIC-CT)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with acute myocardial infarction with or without ST-segment elevation
- Diagnosed with type 2 diabetes
- Initial serum high-sensitivity CRP value greater than 2.0 mg/L
- Clinically obese
- Left ventricular ejection fraction greater than 50%
You will not qualify if you...
- Recent immunosuppressive therapy
- History of ischemic heart disease
- Known allergy to study medications
- Use of study drugs more than 6 months before randomization
- Experiencing diabetic ketoacidosis
- Hemodynamic instability with mean arterial pressure below 60 mmHg on vasopressors
- Pregnant women
- History or current diagnosis of cancer
- Documented active infections such as pneumonia or urinary tract infections
- Pancreatitis
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Unidad Medica de Alta Especialidad No. 1, Bajío
León, Guanajuato, Mexico, 37260,
Actively Recruiting
Research Team
H
Hilda Elizabeth Macías-Cervantes, Ph.D.
CONTACT
R
Rodolfo Guardado-Mendoza, Ph.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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