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Clinical Trials in Canada / NCT06589466
Active, not recruiting Observational

Preoperative Optimization of Diabetic Patients

NCT06589466 · tracked via the Priya Life Science Canada tracker
Phase
Observational
Started
2025-01-22
Last updated
2026-05-06

Condition(s) studied

DiabetesSurgery Related Complications Rate

Investigational drug(s) / intervention(s)

Surgery

Surgery: this study in observational study, no intervention.

Study summary

Diabetic patients, as part of preoperative evaluation, should have glycated hemoglobin (HbA1C) measured. HbA1C provides information on longterm glucose control. There is a suggestion in the literature that elevated A1C levels predict a higher rate of postoperative adverse events, including infections, myocardial infarction, and mortality. It is unclear whether chronic glycemia, as reflected in raised HbA1C level, is the risk factor for adverse perioperative events or whether it is a surrogate measure for poor perioperative glucose management. Conversely, in a retrospective analysis of 431,480 surgeries perioperative glucose was predictive of increased 30-day mortality, but that HbA1C was a less useful predictor of this measure. In our experience of at the University of Alberta Preadmission Clinic there is significant variability with respect to whether diabetic patients have a valid HbA1C measurement i.e. within 3 months of surgery. If a valid measurement is present, there is also considerable variability with respect to diabetes control.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Age 18 or greater * Having any surgical procedure at any hospital in Alberta Exclusion Criteria:

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Alberta Edmonton Alberta

More University of Alberta trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06589466 on ClinicalTrials.gov ↗ ← All trials in Canada