Ireland
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Starting soon Observational

Prognostic Value of the LVOT VTI in STEMI Patients Undergoing PPCI

NCT07114978 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2025-08-01
Last updated
2025-08-11

Condition(s) studied

LVOT VTISTEMI - ST Elevation Myocardial Infarction (MI)Primary Percutaneous Coronary Intervention

Investigational drug(s) / intervention(s)

Echocardiography

Echocardiography: simple, bedsided, non-invasive

Study summary

* To determine whether LVOT VTI \< 15 cm predicts the development of in-hospital cardiogenic shock or need for vasopressors in STEMI patients undergoing primary PCI.
* To assess association of LVOT VTI with other adverse outcomes (in-hospital death, heart failure, arrhythmias, need for mechanical ventilation, prolonged hospital stay).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Adult patients (≥18 years), diagnosed with acute STEMI according to current ESC guidelines(3) and undergoing primary PCI within 24 hours of symptom onset. 2. Patients undergo transthoracic echocardiography within 24 hours of admission. Exclusion Criteria: 1. Presence of significant aortic valve disease (e.g., severe aortic stenosis or regurgitation). 2. LVOT obstruction or hypertrophic cardiomyopathy. 3. Poor echocardiographic window. 4. Refusal to participate.

Primary outcome measure(s)

  • Incidence of cardiogenic shock in patients with LVOT VTI < 15 cm — Through hospital stay (up to 3 days)
    Cardiogenic shock defined per ESC 2023 criteria (SBP \<90 mmHg for ≥30 minutes plus signs of hypoperfusion, or need for vasopressors/inotropic support). Assessed during hospital stay in relation to baseline LVOT VTI. Unit of Measure: Percentage of patients (%)

Trial sites (1)

FacilityCityRegionStatus
Assiut University Asyut Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07114978 on ClinicalTrials.gov ↗ ← All trials in Egypt