Clinical Trials Directory

Trials / Completed

CompletedNCT06338111

Can we Improve Mortality Prediction in Patients With Sepsis in the Emergency Department

Status
Completed
Phase
Study type
Observational
Enrollment
67 (actual)
Sponsor
Iuliu Hatieganu University of Medicine and Pharmacy · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

This study aims to identify the prognostic role of procalcitonin (PCT), soluble Triggering Receptor Expressed on Myeloid Cells-1 (sTREM-1), the soluble form of the urokinase plasminogen activator receptor (suPAR), highly sensitive C-reactive protein (hs-CRP), Interleukin-6 (IL-6), and azurocidin 1 (AZU1) in 28-day mortality for patients with sepsis in Emergency Department.

Detailed description

The levels of the specified biomarkers were measured upon patient arrival at the Emergency Department (ED) and analyzed their correlation with 28-day mortality. The values of these biomarkers were monitored over the initial three days following admission to the ED, aiming to explore their potential in guiding the de-escalation of antibiotic treatment. Considering their prognostic significance, the main goal is to develop a novel scoring system tailored for use in the emergency department setting.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTELISA Sepsis Biomarkers dosageObservational

Timeline

Start date
2020-11-09
Primary completion
2022-12-06
Completion
2023-04-30
First posted
2024-03-29
Last updated
2024-06-07

Locations

1 site across 1 country: Romania

Source: ClinicalTrials.gov record NCT06338111. Inclusion in this directory is not an endorsement.