stresshyperglycemie
Conditions
Interventions
None listed
Sponsors
Academisch Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: * Willing and able to give written informed consent * Scheduled for ambulant surgery * Age 18-85 years
Exclusion criteria
Exclusion criteria: * Any condition that the local investigator feels would interfere with trial participation or the evaluation of results
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary endpoints will be mean glucose change during ambulant surgery as compared to presurgery fasting glucose, proportion patients reaching a glucose value of * 7.8 mmol/l during admission, association between patients with glucose of * 7.8 mmol and seeking any medical help within the first 30 days after discharge. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints will include mean change in glucose during surgery analyzed with specific tests; predictive regression model for perioperative hyperglycaemia; and the association between glucose change and any complication within the first 60 days after discharge. | — |
Countries
Netherlands
Outcome results
None listed