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Active, not recruiting Not applicable

Clinical Usefulness of a Multi-analyte Immunoassay for Distinguishing Bacterial and Viral Infections in Children

NCT06852846 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2024-09-23
Last updated
2025-02-28

Condition(s) studied

Febrile Illness

Investigational drug(s) / intervention(s)

Biological sample

Biological sample: Biomarker test for tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), interferon gamma-inducible protein of 10 kDa (IP-10), and C-reactive protein

Study summary

Fever can be a clinical manifestation present in pediatric infections, posing a challenge for the doctor who must decide whether or not to prescribe an antibiotic therapy. Routine blood tests can assist the doctor in making a decision, although their response times often do not allow for timely therapeutic decisions. Therefore, there is an increased risk of inappropriate prescribing antibiotics for children with viral infections, which contributes to the increase in antibiotic resistance. There is evidence suggesting the effectiveness of certain biomarkers in distinguishing viral from bacterial forms. Biomarkers of potential interest include tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), interferon gamma-inducible protein of 10 kDa (IP-10), and C-reactive protein. The combination of those tests could distinguish between bacterial and viral infections with 90-94% sensitivity, 88-92.8% specificity, 59-81% positive predictive value and 97-98.8% negative predictive value. This is prospective study using biological samples that aims to evaluate the best diagnostic algorithm for obtaining an early and accurate etiological diagnosis (bacterial infection vs viral infection) of a febrile pediatric patient presenting at the Emergency Department, by comparing the standard algorithm with the diagnostic algorithm integrated with the results of the multi-analytic test.

Eligibility

Sex
ALL
Min age
3 Months
Max age
18 Years
Healthy volunteers
No
Inclusion criteria: * Age ≥ 3 months and \< 18 years * Access to the Emergency Department during the study period * Fever (body temperature ≥38°C) for less than 7 days * Absence of an infectious focus or symptoms affecting the respiratory tract Exclusion criteria: * Fever for more than 7 days * Antibiotic therapy for ≥ 48 hours * Acute gastroenteritis * HBV (hepatitis B virus) or HCV (hepatitis C virus) infection * Active oncologic pathology * Metabolic pathology * Trauma or major surgery within the past 7 days

Primary outcome measure(s)

  • Percentage of patients with concordance between biochemical test result and clinical diagnosis — From the date of enrollment to the date of diagnosis

Trial sites (1)

FacilityCityRegionStatus
Meyer Children's Hospital IRCCS, Firenze Florence Italy
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06852846 on ClinicalTrials.gov ↗ ← All trials in Italy