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RECRUITING
NCT07060560

Presepsin Diagnostic Performance in Severe Burn Sepsis

Sponsor: Dohern Kym

View on ClinicalTrials.gov

Summary

This study enrolls approximately 270 adult patients with severe burns covering at least 20% of total body surface area to evaluate how well the blood biomarker presepsin diagnoses sepsis early in this high-risk population. Sepsis-a life-threatening condition caused by an exaggerated immune response to infection-is particularly urgent to detect promptly in burn patients. Participants will undergo blood tests for presepsin at predefined time points, and these results will be compared to C-reactive protein (CRP), procalcitonin (PCT) levels, Sepsis-3 clinical criteria, and blood culture findings. The primary goal is to measure presepsin's sensitivity and specificity for sepsis detection, thereby determining its diagnostic accuracy. Findings from this study may enable faster sepsis treatment in severe burn patients and improve clinical outcomes.

Official title: Prospective Observational Study to Evaluate the Diagnostic Accuracy of Presepsin for Sepsis in Severe Burn Patients

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

138

Start Date

2025-05-01

Completion Date

2026-05-01

Last Updated

2025-08-11

Healthy Volunteers

No

Conditions

Locations (1)

Hangang Sacred Heart Hospital, Hallym University Medical Center

Seoul, Seoul, South Korea