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Clinical Trials/NCT07662980
NCT07662980Not yet recruitingNot Applicable

The Prevalence of Hyperglycemia in Surgical Patients With Pre-diabetes

University of Calgary1 site in 1 country750 target enrollmentStarted: May 1, 2027Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
750
Locations
1

Study Overview

Brief Summary

The goal of this study is to measure the prevalence and risks of hyperglycemia in surgical patients with prediabetes. The main questions it aims to answer are:

  • What is the prevalence of hyperglycemia in surgical patients with prediabetes?
  • What is the relative risk of postoperative complications associated with hyperglycemia?

To answer these questions, surgical patients with prediabetes will undergo universal glucose measurement in the perioperative period. Glucose data will be analyzed in conjunction with electronic health record (EHR) data describing patient outcomes.

Detailed Description

Background

Day-of-surgery and postoperative ('perioperative') hyperglycemia are modifiable risk factors for complications after non-cardiac surgery, including surgical site infections, 30-day readmissions, and mortality. Data from Alberta suggests perioperative hyperglycemia is common among people without diabetes, affecting about 13% of people with prediabetes on the day-of-surgery and 18% of people without diabetes after surgery. Paradoxically, the risks of perioperative hyperglycemia appear to be two-times greater for people with prediabetes than for people with diabetes and the reasons for this are unknown. Current estimates of the prevalence of perioperative for people with prediabetes are limited. Understanding the true prevalence would inform individual decision-making around surgery, the need for further research about the true association of hyperglycemia and adverse outcomes, and clinical decisions about the utility of measuring glucose for all people with prediabetes around the time of surgery.

Objectives

This prospective cohort study will establish the prevalence of perioperativehyperglycemia in people with prediabetes undergoing scheduled (elective and urgent) non-cardiac surgeries. This information will inform:

  1. Patients, to better understand their individual risks of elective surgery.
  2. Clinicians, on the need for perioperative glucose measurement for patients with prediabetes.
  3. Researchers, on the need for and design of further studies.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Hemoglobin A1c measurement between 6 and 6.4%
  • Scheduled for non-cardiac surgery

Exclusion Criteria

  • Pregnancy
  • Any formal diabetes diagnosis
  • Current use of medications that influence blood glucose regardless of the indication
  • Undergoing cardiac, intracranial neurosurgery, bariatric, or pancreatic surgeries

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Shannon Ruzycki

Assistant Professor

University of Calgary

Study Sites (1)

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