Scientists dive deep into Body's battle with COVID-19 and flu
NCT ID NCT05557539
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This completed study collected blood, urine, and nasal swab samples from 249 adults—some with COVID-19, some with the flu, and healthy controls—at two time points. Researchers used a systems biology approach to analyze the data, aiming to understand why people respond differently to these infections. The goal is to improve personalized care for future patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this research could help doctors better predict and personalize treatment for patients with COVID-19 or flu based on their unique biological responses.
- What could go wrong
- This is an observational study that only collected samples and analyzed data—it does not test any treatment. The findings may not lead to immediate clinical changes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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249 people
The number who actually took part.
- Started
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Feb 2022
- Finished
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Jun 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * For all: (1) 18 years or over; (2) Patient or legal representative have provided informed consent. * Cases: Reverse-transcriptase polymerase chain reaction (RT-PCR) confirmed symptomatic SARS-CoV-2 infection. * Controls : 1. Patient presenting with acute respiratory failure: (1) Patient presenting with hypoxemic respiratory failure diagnosed by the treating physician and influenza proven as the cause of the respiratory failure; (2) active SARS-CoV-2 infection excluded by RT-PCR and deemed non-probable by the treating physician. 2. Healthy controls : (1) Patients presenting without acute respiratory failure (ie. SpO2 \>93%); (2) no RT-PCR or antigen rapid test proven SARS-CoV-2 infection within the last 6 months; (3) no active respiratory tract infection. 3. Dexamethasone controls: Patient presenting to the day hospital for an upper or lower limb surgery and who will receive dexamethasone in this context. The criteria for healthy controls also apply. Exclusion Criteria: * For all: (1) \<18 years old ; (2)unwilling to provide informed consent; (3) pregnancy at the time of inclusion * For cases: Asymptomatic infection * For controls: 1. Active COVID-19 infection diagnosed by RT-PCR or suspect according to the treating physician at the time of inclusion, 2. For healthy controls: Acute or chronic respiratory failure. 3. Patient currently receiving dexamethasone (i.e. before study inclusion). The criteria for healthy controls also apply.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Cliniques Universitaires Saint-Luc
Brussels, 1200, Belgium
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Other studies related to the condition(s) this trial covers.
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