Actively Recruiting
Combination of Leukocyte Cell Surface Biomarkers Measured by Cytometry, to Differentiate Bacterial From Viral Infections in Emergency Department: a Multicentric Cohort for the Validation of Diagnostic Performances
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-01-13
500
Participants Needed
3
Research Sites
65 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The characterization of the bacterial or viral etiology of an infectious event is required for both isolation decisions and rationale use of antibiotics. In emergency room (ER), the direct identification of the causal pathogen is rarely available in real-time. Alternative is the identification of the host-response to either a bacterial or viral infection. One of this host-response is the expression of peripheral leukocytes cell surface markers, measured by flow cytometry. Investigators and others have reported the high diagnostic performances of combination of cell surface biomarkers to differentiate bacterial from viral infection. The CYTOBACT study aims to confirm on a 500 patients multicentric cohort (200 having already been collected during another study: SEPTIMET), the best combinations for this diagnostic issue. The study will be conducted in 3 emergency departments of APHP hospitals network in Paris, France. Patients with a suspicion of infection will be proposed to participate. No intervention will be introduced during the routine care in the (ER) which will be let at the discretion of the treating emergency physician. During the routine blood sampling in the ER, an additional 30 ml volume of whole blood will be collected, centrifugated, aliquoted and stored at -80°C for further measurement of the expression of a panel of cell surface markers. The participants will be followed up during their hospitalization (if any) and no longer than 28 days. Clinical data at admission, usual blood tests and all microbiological investigations performed during the hospital stay will be recorded into an electronic case record form (eCRF). Based on all those recorded data (excepted the results of flow cytometry for cell surface biomarkers) 2 independent adjudicators will qualify the infectious episode into bacterial,viral or no infection, and (if any) into infection, sepsis or septic shock (according to Sepsis 3.0 definitions). Using different "machine learning" statistical tools, all the combination of the cell surface biomarkers will be tested to select those with the highest performance to differentiate bacterial from viral infection.
CONDITIONS
Official Title
Combination of Leukocyte Cell Surface Biomarkers Measured by Cytometry, to Differentiate Bacterial From Viral Infections in Emergency Department: a Multicentric Cohort for the Validation of Diagnostic Performances
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years old or older
- Attending one of the participating emergency departments from Monday to Friday between 8:30 am and 3:00 pm
- Suspected infection defined by measured temperature above 38°C or microbiology test ordered during routine care
- Having blood sampling during routine care
- Informed and expressed non-opposition to participate
You will not qualify if you...
- Pregnancy
- No social insurance
- Prisoners
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 3 locations
1
Service des urgences, Lariboisière
Paris, France, 75010
Not Yet Recruiting
2
Service des urgences, Saint-Antoine
Paris, France, 75012
Not Yet Recruiting
3
Service des urgences, Pitié Salpêtrière
Paris, France, 75013
Actively Recruiting
Research Team
L
laetitia Velly, MD
CONTACT
P
Pierre Hausfater, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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