Prognostic Value of the LVOT VTI in STEMI Patients Undergoing PPCI
Condition(s) studied
Investigational drug(s) / intervention(s)
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| Assiut University | Asyut | Egypt |
More Assiut University trials in Egypt
Other trials for the same condition
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