Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07448805

Accuracy and Safety of the Syai Tag System for Continuous Glucose Monitoring in Intensive Internal Care Unit

Led by University Medical Centre Maribor · Updated on 2026-03-04

100

Participants Needed

1

Research Sites

64 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the accuracy and safety of the new Syai Tag system for continuous glucose monitoring in patients admitted to the intensive internal care unit. This study focuses on people with diabetes and other critical illnesses who need close blood sugar monitoring to prevent complications. The trial involves patients in intensive care who require blood sugar monitoring during their stay, with the aim to compare the new continuous glucose monitoring sensors against routine blood sugar tests. Participants will have two small Syai Tag sensors placed on their upper arms to continuously measure their blood sugar levels. These sensor readings will not be visible to medical staff. At the same time, healthcare professionals will carry out routine blood sugar measurements using arterial blood samples. The study will include at least 100 patients and monitor glucose levels from admission up to 14 days or until discharge. The procedure is safe, painless, and patients will continue to receive the usual standard of care. During the study, researchers will track the percentage of time the sensors function properly while in the ICU and compare the glucose values from the sensors to arterial blood gas glucose measurements. Participants will be monitored closely during their ICU stay, which is expected to last more than 24 hours. The study focuses on safety and accuracy while ensuring participants' care remains consistent throughout the trial.

CONDITIONS

Official Title

Accuracy and Safety of the Syai Tag System for Continuous Glucose Monitoring in Intensive Internal Care Unit

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Admission to the intensive care unit
  • Expected ICU stay more than 24 hours
  • Presence of an arterial line
Not Eligible

You will not qualify if you...

  • Age under 18
  • Pregnancy
  • Skin changes that prevent sensor application

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

UMC Maribor

Maribor, Slovenia, 2000

Actively Recruiting

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Research Team

N

Nika Kravos Tramšek, MD PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DEVICE_FEASIBILITY

Number of Arms

1

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