- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT04405726
Prognostic Factors of COVID19 (Covid-HUS)
Study of Clinical, Biological and Genetic Prognostic Factors of SARS-CoV-2 Infection in Patients Admitted in the Strasbourg University Hospitals
COVID-19 is an emerging disease, for which no specific treatment options are currently available. Since the end of February 2020, and due to a SARS-CoV-2 superspreading event (religious meeting), the Strasbourg University Hospital (HUS) had faced a sudden increase of the number of COVID-19-positive patients in serious condition requiring hospitalization. At the same time, many people develop only mild or moderate symptoms. To date, the prognostic factors for the course of SARS-CoV-2 infection are unknown. The primary purpose of the "COVID-HUS" protocol is to investigate viral and host-related factors to understand the pathophysiology of COVID infection and to open the way for new diagnostic, prognostic and therapeutic strategies against SARS CoV-2 .
The secondary objectives are
- Monitoring of viral replication of SARS-CoV-2 in the blood and respiratory tract in infected patients
- Monitoring of the humoral and cellular response directed against SARS-CoV-2
- Identification of factors leading to significant and / or prolonged viral replication of SARS-CoV-2 in the blood or respiratory samples
- Evaluation of the benefit of possible treatments implemented following the diagnosis of SARS-CoV-2 infection
- Exploration of the B and T immune repertoire sequences targeting SARS-CoV-2 in infected patients
- Typing of the HLA system in infected patients
Studieoversikt
Status
Forhold
Studietype
Registrering (Forventet)
Kontakter og plasseringer
Studiesteder
-
-
-
Strasbourg, Frankrike, 67091
- Rekruttering
- Service de Virologie - Hôpital Civil
-
Underetterforsker:
- Yvon Ruch, MD
-
Ta kontakt med:
- Samira FAFI-KREMER, PharmD, PhD
- Telefonnummer: 33.3.69.55.14.38
- E-post: Samira.fafi-kremer@chru-strasbourg.fr
-
Hovedetterforsker:
- Samira FAFI-KREMER, PharmD, PhD
-
Underetterforsker:
- Floriane GALLAIS, MD
-
Underetterforsker:
- Ilies BENOTMANE, MD
-
Underetterforsker:
- Héloïse DELAGREVERIE, MD
-
Underetterforsker:
- Morgane SOLIS, MD
-
Underetterforsker:
- Eric SOULIER, InG
-
Underetterforsker:
- François Danion, MD
-
Underetterforsker:
- Aurélie VELAY, MD
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
Inclusion Criteria:
- Adult and pediatric with suspicion or a confirmed SARS-CoV-2 infection
- Patient who has signed a non-opposition form (or a form signed by a family member or a support person if the seriousness of the patient's condition and the emergency situation do not allow it) or who has given his oral agreement to the doctor
Exclusion Criteria:
- Patient's explicit refusal to participate
- Subject deprived of liberty or subject to the protection of justice
- Subject under guardianship or trusteeship
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Observasjonsmodeller: Bare etui
- Tidsperspektiver: Annen
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Clinical Presentation and Incidence of Covid-19 Infection in patients hospitalised in Strasbourg Hospital
Tidsramme: From 1st March 2020 to 1st March 2021
|
From 1st March 2020 to 1st March 2021
|
Samarbeidspartnere og etterforskere
Etterforskere
- Studieleder: Samira FAFI-KREMER, PharmD, PhD, Laboratoire de Virologie Plateau Technique de Microbiologie
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- 7760
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .