Emergencies Clinical Trial
— RECOPOfficial title:
Emergency Management in a Dedicated Respiratory Unit of Patients With a Possible COVID-19 Infection (Unit "COVID Possible")
NCT number | NCT04371328 |
Other study ID # | RC31/20/0094 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | March 13, 2020 |
Est. completion date | June 30, 2020 |
Verified date | October 2021 |
Source | University Hospital, Toulouse |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
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.
Status | Completed |
Enrollment | 1860 |
Est. completion date | June 30, 2020 |
Est. primary completion date | June 5, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 15 Years and older |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
France | University Hospital of Toulouse | Toulouse |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Toulouse |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Virological status | Virological status will be collected by a phone call at the patient | 30 days | |
Other | Mortality status | Mortality status will be collected by a phone call at the patient | 30 days | |
Primary | Describe the characteristics of patients admitted to reCOP units according to their virological status vis-à-vis COVID-19 | The virological condition will be taken with PCR tests on naso-pharyngeal samples or on sputum for patients taking | 30 days | |
Secondary | Develop a predictive model of the risk of being COVID for patients admitted to the emergency room for dyspnea | demographic variables, usual history and treatments, episode characteristics (symptomatology, evolution, treatment taken) and data from the initial clinical examination will be collected by doctor | 0 days |
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