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Clinical Trial Summary

Sepsis is a complex syndrome that causes lethal organ dysfunction due to an abnormal host response to infection. No drug specifically targeting sepsis has been approved. The heterogeneity in sepsis pathophysiology hinders the identification of patients who would benefit, or be harmed, from specific therapeutic interventions. Recent clinical genomics studies have shown that sepsis patients can be stratified as molecular endotypes, or subclasses, with important clinical implications. Classifying sepsis patients as molecular endotypes revealed that a poor prognosis endotype was characterized by immunosuppression and septic shock. Against this backdrop, the study hypothesis is that a poor prognosis for sepsis is defined by a molecular endotype reflecting impaired innate immune and endothelial barrier integrity in the primary anatomical site of infection.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06287684
Study type Observational [Patient Registry]
Source Mater Dei Hospital, Malta
Contact Brendon Scicluna, Ph.D.
Phone +35623401882
Email brendon.scicluna@um.edu.mt
Status Recruiting
Phase
Start date September 13, 2023
Completion date December 30, 2025

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