Blood test ratios may reveal ICU death risk
NCT ID NCT07242027
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at 212 critically ill adults in one ICU to see if three blood test ratios could predict death. The ratios compare lactate, CRP, and procalcitonin to albumin levels. Researchers will check if these ratios are linked to survival and find cut-off values to help doctors spot high-risk patients early.
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 give doctors a simple tool to quickly identify the sickest ICU patients and prioritize care.
- What could go wrong
- This is a small, single-center retrospective study, so results may not apply to all ICUs. The ratios are not proven to improve patient outcomes yet.
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.
- Participants
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212 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Sep 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.
Who is studied
Adult patients admitted to the ICU. Data collected retrospectively from clinical records (AMMS system).
- 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 years * Admission to ICU in 2024 * Availability of data for lactate, CRP, procalcitonin, and albumin Exclusion Criteria: * Missing outcome data (e.g. unknown survival status) * Lack of laboratory parameters necessary for ratio calculation
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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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Department of Acute Medicine, Faculty of Medical Sciences in Zabrze, Medical University of Silesia in Katowice, Poland
Zabrze, Silesian Voivodeship, 41-800, Poland
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