NCT07268391Recruiting
Using Advanced CT Scans and Blood Markers to Better Understand Heart Damage and Recovery After a Heart Attack
SPEctral CT and miRna In Acute Myocardial Infarction for Comprehensive Adverse Remodeling Evaluation
Source: ClinicalTrials.gov · Last updated 11 Aug 2026
Brief summary (registry, in English)
Acute myocardial infarction with ST-segment elevation (STEMI) remains a leading cause of morbidity and mortality worldwide. Although advances in reperfusion therapy have reduced early mortality, many patients later develop adverse ventricular remodeling (AVR), which increases the risk of heart failure and cardiovascular death. Current imaging methods, such as echocardiography and cardiac magnetic resonance (CMR), provide valuable prognostic information but have limitations in availability, cost, and their ability to predict AVR early and individually. Spectral computed tomography (CT) is an emerging imaging technique that can characterize myocardial tissue, quantify infarct size, assess microvascular obstruction, and detect complications, with lower contrast and radiation requirements compared to conventional CT. In parallel, circulating microRNAs (miRNAs) have been identified as stable and non-invasive biomarkers that reflect key biological processes in post-infarction remodeling. Several miRNAs are linked to fibrosis, apoptosis, and ventricular remodeling, suggesting their potential to complement imaging findings in risk prediction. This study proposes a multicenter, prospective cohort of patients with STEMI and reduced left ventricular function to evaluate whether combining spectral CT tissue characterization with serum miRNA profiling can improve early prediction of AVR. The main objective is to generate and validate a multiparametric prognostic model integrating imaging and molecular biomarkers to identify high-risk patients who may benefit from closer monitoring and tailored therapeutic strategies.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 95 (estimated)
- First submitted
- 18 Nov 2025
- Start date
- 15 Sept 2025
- Primary completion date
- Jan 2027
- Lead sponsor
- Instituto de Investigación Biomédica de Salamanca
- Diseases
- Coronary artery disease
- NCT number
- NCT07268391
What you commit to
- Study type: Interventional
- Planned participants: 95
- From 15 Sept 2025 to the primary completion date, Jan 2027
- 4 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Prior myocardial infarction or known cardiomyopathy.
Other illness
- Life expectancy \<1 year due to non-cardiac conditions.
Lab values
- Chronic kidney disease with eGFR \<30 mL/min/1.73 m².
Other
- Contraindication to iodinated contrast media.
- Contraindication to CT or MRI imaging.
Who the study is looking for
- Adults ≥18 years.
- First STEMI treated with primary PCI.
- Left ventricular ejection fraction (LVEF) ≤45% during index hospitalization.
- Ability to provide informed consent.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hospital Ramón y Cajal Coordinator of this site? Confirm its status | Madrid | Spain | Recruiting |
| Hospital La Princesa Coordinator of this site? Confirm its status | Madrid | Spain | Recruiting |
| Complejo Asistencial Universitario de Salamanca Coordinator of this site? Confirm its status | Salamanca | Spain | Recruiting |
| Hospital Clinico Universitario de Valencia Coordinator of this site? Confirm its status | Valencia | Spain | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.