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Diagnostic and Prognostic Biomarkers of Sepsis

Evaluation of the Role of sTREM-1 and sUPAR Biomarkers as a Diagnostic Tool and Prognostic Predictor in Sepsis Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04767893
Enrollment
67
Registered
2021-02-23
Start date
2019-06-14
Completion date
2020-12-28
Last updated
2021-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sepsis

Keywords

sTREM-1, sUPAR, CRP

Brief summary

This study aims to evaluate sepsis biomarkers as soluble triggering receptor expressed on myeloid cells 1 (sTREM-1) and soluble urokinase plasminogen activator receptor (sUPAR) in diagnosis of sepsis in comparison to the traditional blood culture and C-reactive protein (CRP) and to evaluate the prognostic value of these biomarkers in comparison to sequential organ failure assessment score (SOFA score), Acute Physiology and Chronic Health Evaluation II ( APACHI score), 28 day mortality.

Detailed description

Sepsis is usually diagnosed in patients have clinically suspected infections with systemic inflammatory response syndrome (SIRS) manifestations. Patients with SIRS as those with trauma or stroke have the same classic infection signs such as fever and elevated leukocytic count, as long as the microbiological diagnosis is the ultimate diagnostic method, but it has poor sensitivity with delayed results. New biomarkers such as sTREM-1 and sUPAR can be used for rapid diagnosis of sepsis and differentiating it from non infectious inflammatory syndromes. Also these soluble biomarkers can be used for predicting the prognosis of sepsis patients

Interventions

None listed

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
19 Years to 70 Years

Inclusion criteria

* Temperature of \>38oC * Heart rate of \>90 beats/min * Respiratory rate of \>20 breaths/min * Partial pressure of arterial carbon dioxide (PaCO2) of \<32 mmHg * White blood cell (WBC) count of \>12,000 cells/mm3

Exclusion criteria

* HIV patients * Patients with neutropenia \<1000 cells/mm3 * \<18 years of age.

Design outcomes

Primary

MeasureTime frameDescription
Measurement of the serum level of sTREM-1 (ng/L) in the patients with criteria of SIRSin the 1st day after appearance of clinical signs of infectionby ELISAenzyme linked immunosorbent assay
Measurement of the serum level of sUPAR (ng/L) in the ICU patientsin the 1st day after appearance of clinical signs of infectionby ELISAenzyme linked immunosorbent assay
Measurement of the serum level of sUPAR (ng/L) in the patients with criteria of SIRSin the 7th day after appearance of clinical signs of infectionby ELISAenzyme linked immunosorbent assay
Measurement of the serum level of CRP (mg/dl) in the patients with criteria of SIRSin the 1st day after appearance of clinical signs of infectionby turbidimetry

Secondary

MeasureTime frameDescription
Acute Physiology and Chronic Health Evaluation II (APACHE II) score designed to measure the severity of disease for adult patients admitted to intensive care units in the with criteria of SIRSin the 7th day after appearance of clinical signs of infectionan integer score from 0 to 71
The sequential organ failure assessment score (SOFA score) had been used to determine the extent of organ dysfunction of ICU patients with criteria of SIRSin the 7th day after appearance of clinical signs of infection0-\<11

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026