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NOT YET RECRUITING
NCT07510386
NA

CGM After Discharge From Hospital

Sponsor: Icahn School of Medicine at Mount Sinai

View on ClinicalTrials.gov

Summary

This is an investigator initiated prospective, randomized controlled trial which aims to compare two groups of patients with either type 2 or steroid-induced diabetes who are discharged with insulin. The intervention group will use the Libre 3 Plus continuous glucose monitoring (CGM) system at discharge, while the control group will use blinded CGM and fingerstick monitoring. Both the intervention and control groups will wear the sensor for 28 days post discharge and participate in telehealth diabetes management visits. The target enrollment for the study is 65 participants and participants are expected to be in the study for up to 35 days.

Official title: Continuous Glucose Monitoring for Post-discharge Diabetes Management

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

64

Start Date

2026-04

Completion Date

2026-11

Last Updated

2026-04-03

Healthy Volunteers

No

Interventions

DEVICE

Libre 3 Plus continuous glucose monitoring (CGM) system

Use of unmasked CGM after discharge

DEVICE

Blinded Continuous Glucose Monitoring

Masked CGM

BEHAVIORAL

Finger stick

Self-monitoring blood glucose

Locations (1)

Icahn School of Medicine at Mount Sinai

New York, New York, United States