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Continuous Glucose Monitoring Following Hospital Discharge
Sponsor: Kathleen Dungan
Summary
In this 12-week prospective observational cohort study, hospitalized insulin-requiring patients with T2D will receive a Dexcom continuous glucose monitor (CGM) to wear post-hospital discharge. Patients will complete surveys assessing patient-reported outcomes prior to CGM use and following completion of the study. CGM data will be captured by the patient smartphone app and analyzed. Patients will receive personalized CGM targets and alerts for hyperglycemia and hypoglycemia. Customized reports/ decision support will be sent to the usual diabetes provider. The initial observational cohort study design will be followed by an extension phase of 12 weeks in which data on continuation of use and glucose control will be collected but no further reports will be communicated to providers.
Official title: Effect of Continuous Glucose Monitoring Following Hospital Discharge of Patients With Type 2 Diabetes
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
108
Start Date
2022-04-26
Completion Date
2025-12
Last Updated
2025-12-09
Healthy Volunteers
No
Conditions
Interventions
DexCom G6
Wearable continuous glucose monitor
Locations (1)
The Ohio State University Medical Center - Outpatient Care East
Columbus, Ohio, United States