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Emergency Management in a Dedicated Respiratory Unit of Patients With a Possible COVID-19 Infection

Emergency Management in a Dedicated Respiratory Unit of Patients With a Possible COVID-19 Infection (Unit COVID Possible)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04371328
Acronym
RECOP
Enrollment
1860
Registered
2020-05-01
Start date
2020-03-13
Completion date
2020-06-30
Last updated
2021-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emergencies

Keywords

COVID 19, aspecific respiratory symptomatology

Brief summary

This research aims to improve knowledge of the epidemiology of patients consulting in the COvid Possible REspiratory Units (RECOP unit). Indeed, the epidemic linked to COVID19 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. It will be necessary to identify the diagnosis of the dyspneic patient and to define his virological status COVID before referring him to the appropriate units. The investigatory propose an original strategy of dedicating entire care sectors to the care of patients admitted for dyspnea in our ER. These units will be named RECOP units. This study would improve epidemiological knowledge of COVID-19 and ability to receive these patients within the SU.

Interventions

All patients admit in RECOP unit for dyspnea can be included in this study if patient is agree. Then, doctor collects demographic variables, the usual history and treatments, the characteristics of the episode (symptomatology, evolution, treatment taken) and the data from the initial clinical examination will be identified. 30 days after inclusion, virological status and mortality will be collect

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients over the age of 15 admitted to the RECOP unit for dyspnea

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Describe the characteristics of patients admitted to reCOP units according to their virological status vis-à-vis COVID-1930 daysThe virological condition will be taken with PCR tests on naso-pharyngeal samples or on sputum for patients taking

Secondary

MeasureTime frameDescription
Develop a predictive model of the risk of being COVID for patients admitted to the emergency room for dyspnea0 daysdemographic variables, usual history and treatments, episode characteristics (symptomatology, evolution, treatment taken) and data from the initial clinical examination will be collected by doctor

Other

MeasureTime frameDescription
Virological status30 daysVirological status will be collected by a phone call at the patient
Mortality status30 daysMortality status will be collected by a phone call at the patient

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026