Continuous Glucose Monitoring in Patients Undergoing Cardiopulmonary Bypass

Part of paid clinical trials in Winston-Salem, North Carolina.

Sponsor
Wake Forest University Health Sciences
Study ID
NCT06861881
Status
Not Yet Recruiting

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Conditions

  • Glucose Metabolism Disorders (Including Diabetes Mellitus)

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Dexcom G7 Continuous Glucose Monitor — DEVICE
    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.

Study Details

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 Dates

Start date
Jun 30, 2026
Status verified
Jan 2026
Primary completion
Oct 31, 2026
Completion
Oct 31, 2026

Study Design

Enrollment
100 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY

Arms

  • Experimental: Continuous Glucose Monitoring
    All participants will wear the Dexcom G7 continuous glucose monitor continuously during their cardiothoracic surgery and throughout their time admitted to the Cardiovascular Intensive Care Unit.

Primary Outcome Measure

Continuous Glucose Monitoring Accuracy Compared to Point-of-Care Measurements [ Time Frame: Up to Day 10 ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Wake Forest University Health SciencesWinston-SalemNorth Carolina27157
Lynnette Harris, BSN, RN
[email protected]
336-716-8791
Megan Hicks, MD (PRINCIPAL_INVESTIGATOR)

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By research site
Wake Forest University Health Sciences· Winston-Salem, NC

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