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Clinical Trials/NCT04422587
NCT04422587
Completed
Not Applicable

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

University Hospital, Toulouse1 site in 1 country1,860 target enrollmentMarch 13, 2020
ConditionsEmergencies

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Emergencies
Sponsor
University Hospital, Toulouse
Enrollment
1860
Locations
1
Primary Endpoint
Develop a predictive model of the risk of being COVID-19 for patients admitted to the emergency room for dyspnea
Status
Completed
Last Updated
5 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
March 13, 2020
End Date
June 7, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All patients over 15 years admitted to the RECOP unit for dyspnea

Exclusion Criteria

  • Patient admitted to shock for respiratory distress requiring immediate respiratory support.
  • Patient under justice safeguard

Outcomes

Primary Outcomes

Develop a predictive model of the risk of being COVID-19 for patients admitted to the emergency room for dyspnea

Time Frame: inclusion day

demographic variables, usual history and treatments, episode characteristics (symptomatology, evolution, treatment taken) and data from the initial clinical examination will be collected by doctor

Secondary Outcomes

  • Mortality status(30 days)
  • Describe the characteristics of patients admitted to reCOP units according to their virological status(30 days)
  • Virological status(30 days)

Study Sites (1)

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