Hyperglycaemia and Ambulatory Anaesthesia
Completed
- Conditions
- stresshyperglycemie10018424
- Registration Number
- NL-OMON35862
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 1000
Inclusion Criteria
* Willing and able to give written informed consent
* Scheduled for ambulant surgery
* Age 18-85 years
Exclusion Criteria
* Any condition that the local investigator feels would interfere with trial participation or the evaluation of results
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Primary endpoints will be mean glucose change during ambulant surgery as<br /><br>compared to presurgery fasting glucose, proportion patients reaching a glucose<br /><br>value of * 7.8 mmol/l during admission, association between patients with<br /><br>glucose of * 7.8 mmol and seeking any medical help within the first 30 days<br /><br>after discharge.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary endpoints will include mean change in glucose during surgery analyzed<br /><br>with specific tests; predictive regression model for perioperative<br /><br>hyperglycaemia; and the association between glucose change and any complication<br /><br>within the first 60 days after discharge.</p><br>