Could a watchful software save ICU patients from organ failure?
NCT ID NCT07119411
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This trial tests whether a special alert system called ICU Beacon can help doctors in intensive care units detect early signs of organ failure. The study includes about 1,962 adult ICU patients and compares units using the software plus standard care to those using standard care alone. The goal is to see if the software reduces deaths and limits organ damage during the first 28 days in the ICU.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ICU Beacon software (clinician awareness system)
- What this could lead to
- If it works, this software could help ICU teams detect early signs of organ failure sooner, potentially saving lives and reducing severe complications.
- What could go wrong
- This is a single-center trial, and results may not apply to all ICUs. The software is a decision-support tool, not a treatment, so its impact depends on how doctors use it.
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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About 1,962 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2025
- Expected to finish
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Nov 2027
An estimate. End dates often move.
- 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
The study population includes all patients admitted to the Inselspital Bern ICU, not fulfilling any of the exclusion criteria.
- 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: * admission to intensive care unit Exclusion Criteria: * age \< 18 years * presence of documented refused general consent form (at database closure) * admission for the sole purpose of dying/organ donation or evaluation of such
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Inselspital - Universitätsspital Bern
RECRUITINGBern, 3010, Switzerland
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