critical illness associated hyperglycemia
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Patient is at least 18 years old - Patient is admitted to the ICU of the Academic Medical Center, The Netherlands. - Patient has anticipated life expectancy greater than 96 hours - Patient has recent platelet count greater than 30,000 per micro-liter
Exclusion criteria
Exclusion criteria: - Patient currently has a suspected or diagnosed medical condition that, in the opinion of the Investigator, warrants exclusion from the study or prevents the patient from completing the study - Patient is currently participating in another investigational drug or device study - Patient is pregnant, as determined by hospital admission
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameter is the accuracy of subcutaneous CGM glucose measurements. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoint of this study is to train healthcare workers to use of the Medtronic Sentrino® system, and to obtain feedback from the users on the usability of the Medtronic Sentrino® system. | — |
Countries
Netherlands