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Evaluation of the COVID-19 Infection Response in Patients Admitted to the Emergency Department for Dyspnea — EPRICOD  

Emergencies Clinical Trial

Official title:
Evaluation of the COVID-19 Infection Response in Patients Admitted to the Emergency Department for Dyspnea

Clinical Trial Summary

This research aims to improve our knowledge of the epidemiology of patients consulting in the COvid-19 Possible REspiratory Units (RECOP unit). Indeed, the epidemic linked to COVID-19 affects France and impacts its health system. The reception of all intermediate patients will be on the Emergency Structures (SU). Indeed, the French healthcare system centralizes unscheduled urgent care on the ER. The aspecific respiratory symptomatology in "intermediate" patients indicates them all the more at an admission to SU or the diagnostic approach to respiratory difficulty may be carried out. A central issue of this diagnostic strategy will be to be rapid, since the diagnosis will have to be made in the context of significant flows, with a need to quickly refer patients to the most suitable downstream service, while limiting the risk contamination of caregivers and vulnerable patients if a COVID-19 + patient is admitted to an unsuitable service. However, virological tests do not currently allow rapid results for COVID-19. Research project of investigatory aims to develop a predictive model of the risk of being COVID-19 positive for patients admitted to the emergency room for acute dyspnea.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04422587
Study type Observational [Patient Registry]
Source University Hospital, Toulouse
Contact
Status Completed
Phase
Start date March 13, 2020
Completion date June 7, 2020
View Details
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