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Biomarkers of Inflammation and Endothelial Dysfunction in Patients With Myocardial Infarction With Non-obstructive Coronary Arteries

Biomarkers of Inflammation and Endothelial Dysfunction in Patients With Myocardial Infarction With Non-obstructive Coronary Arteries

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06446895
Acronym
IMACORN-INFLI
Enrollment
400
Registered
2024-06-06
Start date
2020-10-01
Completion date
2025-05-31
Last updated
2024-06-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Biomarkers, Endothelial Dysfunction, Inflammation, MINOCA, Myocardial Infarction

Brief summary

Around 10% of patients with myocardial infarction (MI) present with nonobstructive coronary arteries (MINOCA) which pathophysiology is often uncertain. The aim of the study is to evaluate inflammation and endothelial dysfunction biomarkers in MINOCA patients during both acute and stable phases, comparing them with those with MI and obstructive coronary arteries (MICAD).

Detailed description

Prospective observational study in patients with Myocardial Infarction (MI) divided into two groups: MI with obstructive coronary arteries (MICAD) and MI with non-obstructive coronary arteries (MINOCA). Levels of interleukin-6, tumor necrosis factor-alpha, high-sensitivity C- reactive protein, and asymmetric dimethylarginine will be determined at three time points: within the 24 hours from the onset of pain, discharge, and two months after MI. The association of biomarkers, normalized by peak troponin value, with the risk of MINOCA will be evaluated using logistic regression.

Interventions

DIAGNOSTIC_TESTCoronariography

Patients were classified as MICAD or MINOCA by the presence or absence of an epicardial vessel with ≥50% stenosis after performing a coronariography.

Sponsors

Hospital Universitario Getafe
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients admitted with Myocardial Infarction and undergo a coronariography * Patients must sign informed consent.

Exclusion criteria

* Patients who don´t sign informed consent

Design outcomes

Primary

MeasureTime frameDescription
Levels of interleukin-6 (pg/ml) and tumor necrosis factor-alpha (pg/ml)At three time points: within the 24 hours from the onset of pain, on the 5th day of admission, and two months after MI.Levels of interleukin-6 (pg/ml) and tumor necrosis factor-alpha (pg/ml) will be determined.
Levels of endhotelial disfunction biomarkersAt three time points: within the 24 hours from the onset of pain, on the 5th day of admission, and two months after MI.Levels of asymmetric dimethylarginine will be determined
Levels of high-sensitivity C-reactive protein (mg/L)t three time points: within the 24 hours from the onset of pain, on the 5th day of admission, and two months after MI.Levels of high-sensitivity C-reactive protein (mg/L) will be determined.

Countries

Spain

Contacts

Primary ContactMARIA JESUS ESPINOSA, MD
mariajesusespinosapascual@gmail.com636581691
Backup ContactJOAQUIN ALONSO, PHD
joaquinjalonso@gmail.com609208299

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026