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Can a wearable sensor replace fingerstick tests in the ICU?

NCT ID NCT06645873

Knowledge-focused Sponsor: Kim Kamphorst Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at 100 ICU patients to see if a continuous glucose monitor (CGM) works as well as standard fingerstick tests for tracking blood sugar. The goal was to find out if CGM is reliable enough to use in the ICU. Results will help doctors decide if this technology can improve care for critically ill patients.

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

100 people

The number who actually took part.

Started

Dec 2024

Finished

Sep 2025

Lead sponsor

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

18 years and older

Sex

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patients admitted to the ICU * Insulin-dependent as defined in local protocol * Age: ≥ 18 y * Expected length of stay in ICU more than 2 days Exclusion Criteria: * Pregnancy * No informed consent * Therapeutic hypothermia (less than 34 degrees celsius) * Platelet count less than 50,000/μL at time of inclusion * Use of hydroxyurea * Use of acetaminophen more than 4 g/day

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Conditions

The condition(s) this trial relates to.

hyperglycemia hypoglycemia Insulin Resistance

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Hypoglycemia, hyperglycemia

Contacts and locations

Locations

  • Deventer Ziekenhuis

    Deventer, Overijssel, 7416SE, Netherlands

  • Medisch Spectrum Twente

    Enschede, Overijssel, 7512 KZ, Netherlands

  • Zorggroep Twente Almelo

    Almelo, Overijssel, 7609 PP, Netherlands