Continuous Glucose Monitoring in Intensive Care Unit
Condition(s) studied
Investigational drug(s) / intervention(s)
Dexcom G6 continuous glucose monitor: Continuous glucose monitor will be used to measure interstitial glucose and aid in guiding the insulin therapy to achieve target blood glucose range of 6-10 mmol/l. In the control group, blood glucose will be measured according to standards of care and a blinded continuous monitor will be used to compare the time i range between the arms.
Blood glucose measurements according to standards of care: Blood glucose will be measured using point of care glucose meter and standard biochemistry methods. Blinded CGM will be applied to obtain continuous glucose values for post-hoc comparison.
Study summary
Glucose control in ICU patients is challenging and exerts high burden on the nursing staff. Continuous glucose monitors (CGM) are now approved and widely available in the outpatient setting for patients with diabetes mellitus. However, only minimal evidence on CGM performance, reliability and benefit in achieving desired glucose control in the intensive care setting has been gathered so far.
The objective of this study is to assess whether the use of CGM helps to maintain blood glucose levels within the time in range recommended for patients in the intensive care.
In addition, accuracy of the sensor will be evaluated and compared to measurements of blood glucose by standardized biochemistry methods.
Eligibility
Primary outcome measure(s)
- Time in target range of 6-10 mmol/l — From the time of continuous glucose sensor insertion, which will be performed after admission to postoperative ICU, until the discharge from postoperative ICU, approx. 5-7 days
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Institute for Clinical and Experimental Medicine | Prague | Czechia |
More Institute for Clinical and Experimental Medicine trials in Czechia
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05585801 on ClinicalTrials.gov ↗ ← All trials in Czechia