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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
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

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hospital Ramón y Cajal
Coordinator of this site? Confirm its status
MadridSpainRecruiting
Hospital La Princesa
Coordinator of this site? Confirm its status
MadridSpainRecruiting
Complejo Asistencial Universitario de Salamanca
Coordinator of this site? Confirm its status
SalamancaSpainRecruiting
Hospital Clinico Universitario de Valencia
Coordinator of this site? Confirm its status
ValenciaSpainRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.