Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Admission to the intensive care unit
- Expected ICU stay more than 24 hours
- Presence of an arterial line
You will not qualify if you...
- Age under 18
- Pregnancy
- Skin changes that prevent sensor application
AI-Screening
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Trial Site Locations
Total: 1 location
1
UMC Maribor
Maribor, Slovenia, 2000
Actively Recruiting
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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