Actively Recruiting
LUNG INFECTION in ICU
Led by BioMérieux · Updated on 2025-02-12
68
Participants Needed
1
Research Sites
60 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying patients in intensive care units (ICU) who have lung infections, specifically focusing on ventilator-associated pneumonia (VAP). The study aims to understand the differences in immune cells, especially alveolar macrophages and neutrophils, found in blood and lung fluid after an infection. This observational study is designed to explore immune cell patterns before and at the time VAP is diagnosed, providing insights into how the immune system responds during severe lung infections in critically ill patients. The study does not involve experimental treatments but observes patients who meet specific severe illness criteria, such as septic shock from pneumonia or other causes, severe trauma, or major burns. Participants must be adults aged 18 or older, hospitalized in ICU with these conditions, and show certain clinical signs like vasopressor use and organ dysfunction scores. The research focuses on collecting and analyzing samples to measure immune cells in blood and bronchoalveolar lavage (BAL) fluid during the infection period. Participants will undergo assessments that include sampling of blood and BAL fluid to study immune cell patterns related to VAP. The main outcome measured is the immune cell profiles before and at the time of VAP diagnosis. The study involves monitoring these immune responses in severely ill ICU patients, with participation lasting through the infection and diagnosis period. Safety monitoring and consent processes are in place, and the study will continue through June 2027.
CONDITIONS
Brief Title
LUNG INFECTION in ICU (LUNG-I3)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or greater
- Severe ICU patients hospitalized for septic shock caused by pneumonia or other sources
- Severe trauma (level I and II) with Injury Severity Score 65 25
- Burn patients with total body surface area (TBSA) over 20%
- Receiving noradrenaline (NAD) at dose > 0.1 bcg/kg/min
- At least 2 SOFA criteria with score 65 2 points
You will not qualify if you...
- Aspiration pneumonia
- Inability to provide valid written consent by patient or legal representative
- Chronic obstructive pulmonary disease (COPD)
- Smoke inhalation in burn patients
- Participation in another intervention study
- Pregnant or breastfeeding women
- Immunocompromised patients, including recent chemotherapy, hematologic malignancies, organ transplantation, HIV infection, or immunosuppressive treatment
AI-Screening
AI-Powered Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Duration of ICU stay until diagnosis or discharge
Participants who are severe ICU patients are observed to assess immune cell patterns related to lung infection.
Assessments before and at time of ventilator-associated pneumonia diagnosis
Trial Site Locations
Total: 1 location
1
Hopital Edouard Herriot
Lyon, France, 69003
Actively Recruiting
Research Team
J
Jean-François LLITJOS
M
Marie-Angelique CAZALIS
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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