Can a simple blood test predict which COVID patients will get worse?
NCT ID NCT04341792
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study from France enrolled 373 people who came to the emergency room with suspected COVID-19. Researchers checked routine blood markers to see if any could predict which patients would later get worse and need intensive care. The goal was to find simple, low-risk tests to help hospitals manage resources during the pandemic.
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 could help doctors quickly identify which COVID-19 patients are likely to worsen, allowing better use of hospital resources.
- What could go wrong
- This is an observational study, not a treatment trial. It only looks for patterns in existing data, so it cannot prove that any marker directly causes or prevents worsening.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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373 people
The number who actually took part.
- Started
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Apr 2020
- Finished
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Nov 2020
- 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.
Who is studied
Adult population presenting to the emergency department during this pandemic period with symptoms suggestive of Covid-19 infection with no other probable diagnosis.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
-
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: * Clinical criteria for suspicion of Covid-19 in an epidemic period * Consultation in the emergency departement * Non-opposition agree Exclusion Criteria: * impairment related to another identified cause than Covid-19, in particular a rapid diagnostic test flu-positive * Severe patient from the outset with transfer to intensive care within 12 hours of admission to the Emergency Department * No social security coverage (beneficiary or entitled person) * Poor understanding of French * Refusal to participate
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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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Hôpital Roger Salengro, CHU Lille
Lille, 59037, France
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Other studies related to the condition(s) this trial covers.
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