Could a wearable sensor replace fingerstick tests in the ICU?
NCT ID NCT07687368
First seen Jul 07, 2026 · Last updated Jul 08, 2026 · Updated 1 time
Summary
This trial compares continuous glucose monitoring (CGM) with standard fingerstick testing in 400 critically ill ICU patients with high blood sugar. CGM uses a small sensor under the skin to measure glucose every 5 minutes and alerts staff when levels are too high or low. The goal is to see if CGM helps keep glucose in a safe range, reduces dangerous highs and lows, and cuts down on the number of blood tests needed.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Continuous Glucose Monitoring (CGM) device
- What this could lead to
- If it works, CGM could become routine in ICUs, improving patient safety and reducing the need for frequent fingerstick blood tests.
- What could go wrong
- This is a single-center trial, and results may not apply to all ICUs. CGM may not significantly improve outcomes over standard care.
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
-
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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400 people
The number who actually took part.
- Started
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Jun 2025
- Finished
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Jun 2026
- 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: * Aged 18 years or over * Stay in ICU and/or intermediate care * Blood glucose levels \>180 mg/dL (10 mmol/L). Exclusion Criteria: * Pregnancy * Contraindications for the use of CGM (such as skin issues or allergies to adhesives) * End-of-life process
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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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Carrer de Villarroel, 170
Barcelona, Catalonia, 08036, Spain
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Other studies related to the condition(s) this trial covers.
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