Skip to main content
UK clinical trials - updated daily from ClinicalTrials.gov
TrialConnect
← Back to Search
Looking for participantsN/A

Hospitalised COVID-19 Patients Cohort Study in the EuCARE Project

Sponsor: Euresist Network GEIE

NCT ID: NCT05463380

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
standard of care (other)
How long the study runs
Study runs about 56 months (dates as stated)
About the drug or intervention
standard of care — other: The patient will be treated following the satndard of care in the participating units
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
22,000
Started
2022-02-23
Last checked
2024-08

Plain English Summary

What is this study?

  • • Testing a new treatment for covid-19
  • • Clinical study - 22,000 participants
  • • The WP3 hospitalized cohort in EuCARE is an observational multicentre study including collection of retrospective (historical) and prospective data from hospitalized COVID-19 patients followed at 12 clinics from 11 countries from 4 continents

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with covid-19

Where?

  • • Poole - Poole University Hospitals, Dorset

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

The WP3 hospitalized cohort in EuCARE is an observational multicentre study including collection of retrospective (historical) and prospective data from hospitalized COVID-19 patients followed at 12 clinics from 11 countries from 4 continents. In a subset of patients, peripheral blood, viral isolates and/or viral sequences are collected for analysis in WP2 with regards to neutralising antibodies, cellular immunity and SARS-CoV-2 diagnostics. Data and results from analysis of biological material will be analysed by biostatistical methods and with artificial intelligence in WP5. This analysis will focus on the impact on clinical outcome of viral variants / viral sequences as well as the vaccines used and the vaccination schedules.

More detail

Background: Since the start of the COVID-19 pandemic, novel SARS-CoV-2 variants of concern have emerged, some of which have become largely dominant including the B.1.1.7 (alpha), the B.1.617 (delta) and more recently the B.1.1.529 (omicron). The clinical implications of the different variants in unvaccinated and vaccinated persons are still not adequately characterized. The detailed understanding of the interplay between the variants, vaccine immune responses and disease severity is still scarce. Study objectives: Overall objectives are: * to collect data and/or biological material from COVID-19 in-patients in a diverse setting of 12 clinics in 11 countries and 4 continents * to analyse the clinical course of COVID-19 in in-patients in relation to the viral characteristics * to analyse the clinical course of COVID-19 in in-patients in relation to vaccines used and vaccination schedules * to deliver recommendations for optimized clinical management and treatment with special consideration to viral characteristics and to used vaccines Specific objectives are: * To describe the patterns of clinical symptoms, therapeutic interventions and clinical outcome in patients hospitalized from 12 hospitals/clinics, in 11 countries and 4 continents. * To assess the impact of viral variants / viral sequences on the clinical outcome measured as all-cause in-hospital mortality, non-invasive mechanical ventilation/high-flow nasal oxygen, mechanical ventilation, admission to intensive care unit, length of time in intensive care and overall length of hospitalization. * To assess the impact of different vaccines and vaccination schedules on the clinical outcome measured as all-cause in-hospital mortality, non-invasive mechanical ventilation/high-flow nasal oxygen, mechanical ventilation, admission to intensive care unit, length of time in intensive care and overall length of hospitalization. * To assess the impact of viral variants / sequences in response to treatment interventions and the associated clinical outcome * To assess the impact of different vaccines and vaccination schedules in response to treatment interventions and the associated clinical outcome * To provide WP2 in EuCARE with biological material for further studies on viral characteristics and associated immune responses * To provide WP5 in EuCARE with data for further studies using artificial intelligence

COVID-19

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

Treatment history

Treatments you must have had:

  • ✓ by ethical approval

What the study is looking for

  • ✓Hospitalized adult (\>18 years) patients including patients in the emergency ward
  • ✓Positive for SARS-CoV-2 by PCR any time from 14 days before admission date until hospital discharge. Both first and...
  • ✓Having a signed agreement to take part when required by ethical approval
See the full criteria
Inclusion Criteria: * Hospitalized adult (\>18 years) patients including patients in the emergency ward * Positive for SARS-CoV-2 by PCR any time from 14 days before admission date until hospital discharge. Both first and recurrent episodes of COVID-19 will be included. * Having a signed informed consent when required by ethical approval Exclusion Criteria: none

Where Is This Study? (1 UK site)

Poole University Hospitals, Dorset

Poole, United Kingdom

Recruiting
Hospital R&D contact (matched)

Louise Bell

uhd.researchoffice@nhs.net0300 019 8500

How to Get in Touch

FRANCESCA INCARDONA Project Coordinator

Sponsor contact

CONTACT

+393356112830 francesca.incardona@euresist.org
Data sourced from ClinicalTrials.gov · Last verified: 2024-08