Actively Recruiting
Fulminant Cases Among Severe Community-acquired Pneumonia - an Observational Retrospective Study
Led by University of Trieste · Updated on 2024-07-24
1460
Participants Needed
2
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Severe community-acquired pneumonia (CAP) is a major cause of hospital deaths, especially when it progresses rapidly into a condition known as fulminant pneumonia. This rapid worsening can lead to severe acute respiratory distress syndrome (ARDS), acute respiratory failure, and septic shock within hours or days. The true frequency and best treatment approach for fulminant pneumonia remain unclear, partly because pneumonia is often studied separately from related conditions like ARDS and sepsis. The COVID-19 pandemic has highlighted the presence of fulminant pneumonias, increasing the need to understand this condition better. This observational study gathers data from patients hospitalized with severe CAP at five centers between January 2018 and July 2024. Patients included both COVID and non-COVID cases who met specific criteria for severe pneumonia and respiratory distress. Early antibiotic treatment was standard, while corticosteroid use depended on physician decisions or other protocols. The study excluded hospital- or healthcare-acquired pneumonia and patients with advanced chronic illnesses. Participants' clinical information was collected at admission, including oxygen levels, vital signs, age, ICU admission, hospital stay length, and ventilation details. Researchers will analyze mortality rates at 2, 7, 30, and 60 days to assess outcomes. The study seeks to better understand fulminant pneumonia rates and the role of early corticosteroid treatment in severe CAP patients. The total observation period spans from patient admission through at least 60 days for outcome assessment.
CONDITIONS
Brief Title
Fulminant Severe CAP - an Observational Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Severe community-acquired pneumonia according to ATS/IDSA criteria
You will not qualify if you...
- Incomplete outcome data
- Hospital-acquired pneumonia
- Healthcare-acquired pneumonia
- Advanced chronic illnesses such as metastatic cancers or advanced neuromuscular disorders
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - At hospital admission
Participants' clinical and laboratory data are collected at admission to assess their condition with severe community-acquired pneumonia.
1 visit (in-person)
Duration - Up to 60 days
Participants are observed for outcomes including mortality at various timepoints up to 60 days after admission without active intervention.
Follow-up assessments at 2, 7, 30, and 60 days
Trial Site Locations
Total: 2 locations
1
Marco Confalonieri
Trieste, TS, Italy, 34149
Actively Recruiting
2
SC Pneumologia, Azienda Sanitaria Universitaria Giuliano-Isontina
Trieste, Italy, 34126
Actively Recruiting
Research Team
M
MARCO CONFALONIERI, MD
F
Francesco Salton, MD
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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