COMPAS studie
- Conditions
- diabetes mellitusperioperative periodcontinuous glucose sensor
- Registration Number
- NL-OMON24618
- Lead Sponsor
- Academic Medical Centre, university of amsterdam
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 36
Inclusion Criteria
Aged 18-85
-Able to give written informed consent
Exclusion Criteria
-Any condition that the local investigator feels would interfere with trial participation or the evaluation of results
-Allergy for heparin
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The difference in median glucose 1 hour after surgery will be calculated as a measure of glycaemic control during surgery. <br>Furthermore, the difference in proportion of time spent in the target range, time spent above the target range and time spent below the target range between groups will be calculated.<br>
- Secondary Outcome Measures
Name Time Method