Blood samples and health records could reveal why some COVID-19 cases turn severe
NCT ID NCT04352348
First seen Sep 21, 2026 · Last updated Sep 21, 2026
Summary
Researchers in the Ile-de-France region are following adults hospitalized with COVID-19 or suspected of having it. They collect blood samples at admission and, for severe cases, at several later points, and they track health outcomes over time. The goal is to identify which factors predict progression to severe illness and to describe how the disease unfolds, so hospitals can better care for patients during epidemics.
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 researchers identify reliable prognostic factors, doctors could better predict which COVID-19 patients will worsen and direct limited hospital resources to those who need them most.
- What could go wrong
- This observational study can only find associations, not prove cause and effect. The findings may not apply to other regions or future variants, and the blood samples may not reveal clear answers.
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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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2,003 people
The number who actually took part.
- Started
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Mar 2020
- Finished
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May 2022
- 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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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Age ≥ 18 * Patient admitted in an emergency unit or hospitalized, infected with SARS-CoV2 or suspected of being (the recruitment can occured during acute episode or during a follow-up visit) * Written informed consent or emergency procedure * Affiliated to health insurance system Exclusion Criteria: * Refusal of participation * Patient under justice protection measure except guardianship and trusteeship
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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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GH Pitié-Salpêtrière / Service d'Accueil des Urgences
Paris, Île-de-France Region, 75013, France
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Other studies related to the condition(s) this trial covers.
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