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NCT06428318 Clinical Trial

Diagnostic Value of the Biofire®in Community Acquired Pneumonia

Pneumonia Clinical Trial

Official title:
Diagnostic Value of the Biofire® Filmarray Pneumonia Panel Compared to Conventional Sputum Culture in Critically il Patients With Pneumonia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06428318
Other study ID # FMASU MS267/2023
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 15, 2023
Est. completion date April 30, 2024

Study information
Verified date May 2024
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aimed to determine the impact value of the BioFire FilmArray Pneumonia panel compared to conventional sputum culture in critically ill patients with pneumonia.

Description:

the BioFire® FilmArray Pneumonia Panel (BFPP) emerges as a promising candidate for a rapid and multifaceted diagnostic approach. This study compare the diagnostic accuracy, turnaround time, and impact on antibiotic management decisions of BFPP versus conventional sputum culture in critically ill patients admitted to the ICU with suspected pneumonia.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date April 30, 2024
Est. primary completion date April 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Patients admitted to the ICU with community acquired pneumonia Exclusion Criteria: - Age less than 18 years old. - End stage malignant patients, - Patients admitted to the ICU with Acute Lung Injury (ALI). - Patients admitted to the ICU with Acute Respiratory Distress Syndrome (ARDS). - Patients with radiological findings suggesting atypical pneumonia. - Immunocompromised as defined by HIV/AIDS, known immunodeficiency, chronic steroids > 20mg/day Prednisone equivalent, other immunosuppressants. - Solid organ or bone marrow transplant patients, cystic fibrosis. - Unstable psychiatric or psychological condition rendering the subject unlikely to be cooperative or to complete the study requirements.

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• Conventional Sputum culture
Sputum culture was done to patients and they received Antibiotics According to its results
• BioFire Pneumonia Panel (BFPP)
BioFire Pneumonia Panel (BFPP) was done to patients and they received Antibiotics According to its results

Locations
Country Name City State
Egypt Ain Shams University Cairo Abassia

Sponsors (1)
Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary the ICU length of stay The potential correlation between the use of BFPP and its relation to the ICU length of stay Five days after admission
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