COVID-19 Infection in Patients With Hepatocellular Carcinoma

NCT04367805 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 23

Last updated 2024-04-10

No results posted yet for this study

Summary

Since December 2019, a new disease named COVID-19 linked to a new coronavirus, SARS-CoV2 has emerged in China in the city of Wuhan, Hubei province, spreading very quickly to all 5 continents, and responsible for a pandemic. France is the third most affected country in Europe after Italy and Spain. Groups of patients at a higher risk of developing a severe form of COVID-19 have been defined: this include patients with immunosuppressive disease as cancer or patients with advanced cirrhosis of the liver. Coronavirus liver injury had been described with SARS-CoV 1 and MERS-CoV. There is no data on liver damage associated with COVID-19 infection for compensated or decompensated cirrhotic patients. The objectives of this project are to estimate the incidence of COVID-19 in hepatocellular carcinoma population, both hospital and ambulatory, and to study the impact on the frequency of severe forms, the prognosis, but also liver function, and the management of hepatocellular carcinoma, in this context of pandemic

Conditions

Interventions

DIAGNOSTIC_TEST

nasopharyngeal Covid 19 RT-PCR

nasopharyngeal Covid 19 RT-PCR

Sponsors & Collaborators

  • Centre Hospitalier-Universitaire Bondy

    collaborator UNKNOWN
  • University Hospital, Bordeaux

    collaborator OTHER
  • Centre Hospitalier-Universitaire CLICHY

    collaborator UNKNOWN
  • Centre Hospitalier Général CORBEIL-ESSONNE

    collaborator UNKNOWN
  • CHU CRETEIL

    collaborator UNKNOWN
  • University Hospital, Grenoble

    collaborator OTHER
  • University Hospital, Lille

    collaborator OTHER
  • Hospices Civils de Lyon

    collaborator OTHER
  • Poitiers University Hospital

    collaborator OTHER
  • Rennes University Hospital

    collaborator OTHER
  • University Hospital, Rouen

    collaborator OTHER
  • University Hospital, Toulouse

    collaborator OTHER
  • CHU VILLEJUIF

    collaborator UNKNOWN
  • Central Hospital, Nancy, France

    collaborator OTHER
  • Centre Hospitalier Universitaire de Nice

    collaborator OTHER
  • University Hospital, Montpellier

    collaborator OTHER
  • Centre Hospitalier Universitaire, Amiens

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-04-27
Primary Completion
2023-10-01
Completion
2024-10-31

Countries

  • France

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04367805 on ClinicalTrials.gov