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This is an observational prospective multicenter study of patients admitted for acute dyspnea in an emergency department of the participating centers in the Lorraine district.
The primary objective is to assess the outcome of this population according to the cause of acute dyspnea as well as identify the predictors of this outcome, both overall and according to each acute dyspnea cause.
Full description
This observational prospective multicenter study will be conducted using data from electronic medical records, acquired as part of usual care, in patients admitted for acute dyspnea in the emergency department. Clinical, treatment, laboratory and imaging data acquired during the hospitalization (in the emergency department and in the department that admitted the patients following the emergency department stay) will be collected.
Vital status will be recorded at 30 days and 1 year post-admission.
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75,000 participants in 1 patient group
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Central trial contact
Tahar CHOUIHED, MD; Nicolas GIRERD, MD,PhD
Data sourced from clinicaltrials.gov
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