Clinical trials

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Condition / disease
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Status: Not yet recruiting

Evaluating the Accuracy of Multiple Blood Tests to Diagnose Sepsis in Adult Burn Patients

This prospective diagnostic accuracy study evaluates the performance of presepsin and C-reactive protein (CRP) as early biomarkers for suspected sepsis in adult burn patients. From January 2021 to December 2022, 370 patients with ≥20% total body surface area burns admitted to the Burn Intensive Care Unit at Hallym University Hangang Sacred Heart Hospital were screened; 221 met inclusion criteria. At each clinical suspicion of sepsis (≥2 SIRS criteria), venous blood was drawn for simultaneous measurement of presepsin (via chemiluminescent immunoassay) and CRP (via immunoturbidimetric assay). Diagnostic accuracy will be quantified by sensitivity, specificity, positive/negative predictive values, and area under the ROC curve. The goal is to determine whether presepsin outperforms CRP for early sepsis detection in severe burn patients.

Participants needed: 165
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Dohern KymUpdated: Aug 17, 2025Duration: 1 Year
Eligibility criteria

Age 18 years or older. [+3]

Pregnancy. [+3]

Status: Recruiting

Presepsin Diagnostic Performance in Severe Burn Sepsis

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.

Participants needed: 138
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Dohern KymUpdated: Aug 11, 2025Locations: 1Duration: 4 Days
Eligibility criteria

Adults aged ≥ 18 years admitted to Hangang Sacred Heart Hospital Burn ICU with t... [+2]

Inability to undergo research blood draw due to emergent surgery or major trauma... [+3]