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ACTIVE NOT RECRUITING
NCT05360056
NA

Continuous Glucose Monitoring Following Hospital Discharge

Sponsor: Kathleen Dungan

View on ClinicalTrials.gov

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

DEVICE

DexCom G6

Wearable continuous glucose monitor

Locations (1)

The Ohio State University Medical Center - Outpatient Care East

Columbus, Ohio, United States