Clinical Trials Directory

Trials / Completed

CompletedNCT06491004

Evaluation of DiaSorin LIAISON® PTX3 (Long Pentraxin 3) Assay in Patients With Pneumonia

Status
Completed
Phase
Study type
Observational
Enrollment
281 (actual)
Sponsor
Diasorin Italia S.p.A. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

LIAISON® PTX3 is an in vitro chemiluminescent immunoassay (CLIA) intended for the quantitative determination of Long Pentraxin 3 (PTX3) in human plasma samples. LIAISON® PTX3, in conjunction with clinical evaluation and other laboratory findings, may serve as an aid in the determination of disease severity and prognosis of patients with community-acquired (CAP) and hospital-acquired pneumonia (HAP), including ventilator-associated pneumonia (VAP).

Detailed description

Long Pentraxin 3 (PTX3) is an essential protein of innate immunity, produced by myeloid cells, endothelial cells and respiratory epithelial cells, and involved in resistance to selected pathogens and in inflammation. In different pathological conditions (infections of bacterial and viral origin, sepsis, and cardiovascular diseases) and in patients requiring admission to intensive care units (ICUs), PTX3 was detected in high concentrations in the circulation and was associated with disease severity and mortality. PTX3 plasma concentration was found to be an independent prognostic indicator of short-term mortality (28 days) in hospitalized patients with Coronavirus Disease 2019 (COVID- 19) and higher PTX3 levels were found in ICU patients compared to ward patients. Moreover, PTX3 significantly correlated with the inflammatory molecules C-reactive protein (CRP), procalcitonin (PCT), and interleukin (IL)-6. Given the association between PTX3 and inflammatory conditions, especially in the context of lung infections, the study aims to investigate the potential of PTX3 to be used as a severity marker and a prognostic predictor for outcome in patients with community-acquired (CAP) and hospital-acquired pneumonia (HAP), including ventilator-associated pneumonia (VAP).

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTPTX3 assayPTX3 dosage by the in vitro medical device in evaluation.

Timeline

Start date
2021-09-20
Primary completion
2024-03-29
Completion
2024-03-29
First posted
2024-07-08
Last updated
2024-07-08

Locations

2 sites across 1 country: Italy

Source: ClinicalTrials.gov record NCT06491004. Inclusion in this directory is not an endorsement.