About this trial
The objective of this prospective observational study is to describe the epidemiological, clinical and biological characteristics of admitted patients in ICU for severe acute exacerbation of COPD, to assess the different therapeutics used, to evaluate the prognosis of patients with short, medium and long term ( 1 year) and the various factors associated with survival in ICU
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age ≥ 40 years old
COPD documented or strongly suspected
Chronic respiratory symptoms (dyspnoea, cough and/or sputum)
Exposure to a known risk factor for COPD (such as tobacco smoke)
Disqualifiers
Known asthma (according to the criteria of the international "Global initiative for asthma" guidelines)
Patient refusal to participate (information note, application for non-opposition)
Trial population
patients with severe acute exacerbation of COPD admitted in ICU
Trial design
Cohort
Prospective
Treatments tested in this trial
register
Other interventionMulticentre prospective observational register
Treatment groups
Trial outcomes
Primary outcomes
the epidemiological, clinical and biological characteristics of patients admitted to the ICU for a severe acute exacerbation of COPD
to describe the epidemiological, clinical and biological characteristics of patients admitted to the ICU for a severe acute exacerbation of COPD
Sponsors and contacts
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Alexis FERRE
Lead sponsor
Versailles Hospital
Sponsor institution