Perioperative hyperglycaemia and glucose variability during major abdominal surgery

Completed

• Conditions: stress hyperglycaemia; 10018424

• Registration Number: NL-OMON35746
• Lead Sponsor: Academisch Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 400

Inclusion Criteria

- Willing and able to give written informed consent
- Scheduled to undergo major abdominal surgery
- Age 18-85 years

Exclusion Criteria

- Early termination of the procedure
- Conditions necessitating prolonged stay (beyond the first postoperative day) at the recovery room, readmission to the recovery room, or admission to an intensive or medium care unit

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Our main endpoint is the relation between postoperative complications and<br /><br>hyperglycaemia and glucose variability. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary endpoint is the difference in glucose increase and variability<br /><br>between different surgical procedures and treating specialties.</p><br>