Perioperative Continuous Glucose Monitoring

Stopped early · Not applicable

Conditions studied: Diabetes Mellitus

In brief

To evaluate use of continuous glucose monitoring (CGM) technology in the preoperative setting: evaluate feasibility of placement of CGM during preoperative clinic visit with intent to utilize CGM throughout perioperative period.

Key facts

Study ID

NCT05937373

Run by

Wake Forest University Health Sciences

People needed

22

Starts

2023-08-04

Expected to finish

2024-05-21

Last updated by the study team

2025-12-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants that are 18 years of age or older with hyperglycemia and/or diabetes mellitus who will be undergoing surgery at Atrium Health Wake Forest Baptist
• smartphone compatible with Libre 2 phone application

You may not qualify if…

• Pregnant women will not be excluded from this study
• Participants undergoing surgery that would limit the placement of Continuous Glucose Monitoring (CGM) to the posterior aspect of the upper extremity will be excluded from this study
• neurosurgical type of surgery

Where it is running

• Wake Forest Health Sciences — Winston-Salem, North Carolina, United States

Full record on ClinicalTrials.gov

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