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NCT06861881
Continuous Glucose Monitoring in Patients Undergoing Cardiopulmonary Bypass
Conditions: Glucose Metabolism Disorders (Including Diabetes Mellitus)
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 100
Sponsor: Wake Forest University Health Sciences
Location: Wake Forest University Health Sciences Winston-Salem North Carolina
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.
Eligibility Criteria
Inclusion Criteria:
* 18 years of age or older
* Undergoing cardiac surgery with cardiopulmonary bypass at Atrium Health Wake Forest Baptist Medical Center
Exclusion criteria:
* Under 18 years of age
* Pregnant women
* Patients with a contraindication to device placement on the posterior arm, including rash, missing extremity, or existing line or device
Source: ClinicalTrials.gov (NCT06861881). StuddyBuddy aggregates publicly available trial information.
