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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04679025
Other study ID # HREBA.CC-19-0157
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 1, 2019
Est. completion date March 31, 2020

Study information

Verified date December 2020
Source University of Calgary
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Patients with and without diabetes who have postoperative hyperglycemia have worse outcomes than patients with in-target blood sugars. Previous quality improvement work suggests numerous barriers and clinical inertia may contribute to quality gaps in glycemic management for surgical patients. Using a framework for perioperative glycemic management, we sought to measure quality gaps in perioperative glycemic care. This cross-sectional study used administrative data to measure the proportion of surgical patients with and without known diabetes who underwent preoperative hemoglobin A1c measurement, postoperative point-of-care testing for glucose (POCT), had hyperglycemia, and received basal bolus insulin regimens for treatment. We performed an exploratory analysis comparing length of stay (LOS) in patients with and without diabetes who had and did not have postoperative hyperglycemia.


Recruitment information / eligibility

Status Completed
Enrollment 7633
Est. completion date March 31, 2020
Est. primary completion date March 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Underwent inpatient surgical procedure at the Foothills Medical Centre between Apr 1 2019 and March 31 2020 - Stayed in hospital for more than 24-hours after surgery Exclusion Criteria: - Younger than 18 years of age

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exposure - postoperative hyperglycemia
Postoperative hyperglycemia (blood or capillary glucose > 10.0 mmol/L) within 72 hours of a surgical procedure

Locations

Country Name City State
Canada Foothills Medical Centre Calgary Alberta

Sponsors (1)

Lead Sponsor Collaborator
University of Calgary

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of point of care blood glucose measurements in 24-hours after surgery 24-hours post surgery
Primary Proportion of patients who have hyperglycemia blood or capillary glucose > 10 mmol/L 24-hours after surgery
Secondary Proportion of patients who have moderate hyperglycemia blood or capillary glucose 14.0-17.9 mmol/L 24-hours after surgery
Secondary Proportion of patients who have severe hyperglycemia blood or capillary glucose > 18.0 mmol/L 24-hours after surgery
Secondary Hospital Length of stay Hospital length of stay (days) Until study completion (up to one year from surgical procedure)
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