- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04422587
Evaluation of the COVID-19 Infection Response in Patients Admitted to the Emergency Department for Dyspnea (EPRICOD)
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.
Studieoversigt
Undersøgelsestype
Tilmelding (Faktiske)
Kontakter og lokationer
Studiesteder
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Toulouse, Frankrig, 31000
- University Hospital of Toulouse
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
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
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
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RECOP unit patient
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.
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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.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Develop a predictive model of the risk of being COVID-19 for patients admitted to the emergency room for dyspnea
Tidsramme: inclusion day
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demographic variables, usual history and treatments, episode characteristics (symptomatology, evolution, treatment taken) and data from the initial clinical examination will be collected by doctor
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inclusion day
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Virologisk status
Tidsramme: 30 dage
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Virologisk status vil blive indsamlet ved et telefonopkald hos patienten
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30 dage
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Dødelighedsstatus
Tidsramme: 30 dage
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Dødelighedsstatus vil blive indsamlet ved et telefonopkald hos patienten
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30 dage
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Describe the characteristics of patients admitted to reCOP units according to their virological status
Tidsramme: 30 days
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The COVID-19 virological condition will be taken with PCR tests on naso-pharyngeal samples or on sputum for patients taking
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30 days
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Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Paul-Henri Auboiroux, MD, University Hospital of Toulouse
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Patologiske processer
- Coronavirus infektioner
- Coronaviridae infektioner
- Nidovirales infektioner
- RNA-virusinfektioner
- Virussygdomme
- Infektioner
- Luftvejsinfektioner
- Luftvejssygdomme
- Respirationsforstyrrelser
- Lungebetændelse, viral
- Lungebetændelse
- Lungesygdomme
- Sygdomsegenskaber
- Tegn og symptomer, luftveje
- COVID-19
- Nødsituationer
- Dyspnø
Andre undersøgelses-id-numre
- RC31/20/0149
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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Kliniske forsøg med RECOP unit patient
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University Hospital, ToulouseAfsluttet
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Centre Hospitalier St AnneAssistance Publique - Hôpitaux de Paris; Ministry of Health, FranceRekrutteringSlagtilfælde, AkutFrankrig
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University Hospital, GrenobleTIMC-IMAG; Centre Medico Universitaire Daniel Douady (CMUDD)Afsluttet
-
NYU Langone HealthIkke rekrutterer endnu
-
AnthogyrAktiv, ikke rekrutterendeEdentuous | TandimplantaterSpanien, Portugal
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Hospital Universitario ArabaLinde Health Care; Spain:Health Department. Basque Government.Afsluttet
-
University of NebraskaNational Institute of Mental Health (NIMH)Afsluttet
-
Centre for Evidence-Based Practice, BelgiumBelgian Red CrossAfsluttetSlag | ForbrændingerBelgien
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Hospital Universitario Reina Sofia de CordobaSpanish Society of Family and Community MedicineAfsluttet
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Velico MedicalTilmelding efter invitationBlødning | KoagulopatiForenede Stater