Actively Recruiting

Age: 18Years +
All Genders
ID06516601

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Severe community-acquired pneumonia according to ATS/IDSA criteria
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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)

Long-term Monitoring

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

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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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