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Study identifier: NCT07060560 Synced from ClinicalTrials.gov · July 28, 2026
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Presepsin Diagnostic Performance in Severe Burn Sepsis

Condition: Sepsis · Burns  ·  Sponsor: Dohern Kym

PhaseN/A
Planned participants138
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

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Locations (1)

Hangang Sacred Heart Hospital, Hallym University Medical CenterSeoul, Seoul, South KoreaRecruiting

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Source record: clinicaltrials.gov/study/NCT07060560