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NOT YET RECRUITING
NCT06861881
NA

Continuous Glucose Monitoring in Patients Undergoing Cardiopulmonary Bypass

Sponsor: Wake Forest University Health Sciences

View on ClinicalTrials.gov

Summary

The purpose of this research study is to test the accuracy of the Dexcom continuous glucose monitoring device during the cardiothoracic surgical procedure and recovery period in the Cardiac Intensive Care Unit. Readings from the device will be compared with the standard of care blood glucose levels that are obtained during your surgery and postoperatively.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-05

Completion Date

2026-10

Last Updated

2026-03-25

Healthy Volunteers

No

Interventions

DEVICE

Dexcom G7 Continuous Glucose Monitor

Dexcom G7 continuous glucose monitor will be placed prior to cardiac surgery. It will be worn continuously throughout the perioperative period and during the time admitted to the Cardiovascular Intensive Care Unit.

Locations (1)

Wake Forest University Health Sciences

Winston-Salem, North Carolina, United States