Continuous Glucose Monitoring for Outpatient Diabetes Management After Hospital Discharge

Part of paid clinical trials in Nashville, Tennessee.

Sponsor
Vanderbilt University Medical Center
Study ID
NCT06852950
Status
Recruiting

Conditions

  • Hyperglycemia
  • Type 1 Diabetes Mellitus (T1DM)
  • Type 2 Diabetes Mellitus (T2DM)

Eligibility Criteria

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

Interventions

  • Libre 3 Plus Continuous Glucose Monitor — DEVICE
    Subjects in this arm will start using the Libre 3 Plus continuous glucose monitor.
  • Dexcom G7 Continuous Glucose Monitor — DEVICE
    Subjects in this arm will start using the Dexcom G7 continuous glucose monitor.

Study Details

This study aims to improve patient awareness of the utility of continuous glucose monitoring systems in blood glucose monitoring and to improve patient satisfaction regarding diabetes care, particularly in the matter of blood glucose monitoring, at the transitions of care from the inpatient setting to the ambulatory setting.

Key Dates

Start date
Mar 9, 2025
Status verified
Mar 2026
Primary completion
Jan 31, 2027
Completion
Jan 31, 2027

Study Design

Enrollment
60 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER

Arms

  • Experimental: Libre 3 Plus Continuous Glucose Monitor
    Subjects in this arm will start using the Libre 3 Plus continuous glucose monitor.
  • Experimental: Dexcom G7 Continuous Glucose Monitor
    Subjects in this arm will start using the Dexcom G7 continuous glucose monitor.

Primary Outcome Measure

Questionnaire responses regarding patient satisfaction and opinion regarding use of continuous glucose monitoring system [ Time Frame: From enrollment until follow-up telephone visit 2-3 weeks after discharge ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Vanderbilt University Medical CenterNashvilleTennessee37232
Angel Morvant, MD
(615) 343-8332
Angel Morvant, MD (PRINCIPAL_INVESTIGATOR)

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