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
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
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
Where Is This Study? (1 UK site)
Poole University Hospitals, Dorset
Poole, United Kingdom
How to Get in Touch
FRANCESCA INCARDONA Project Coordinator
Sponsor contactCONTACT
