CGM After Discharge From Hospital
Starting soon · Not applicable
Conditions studied: Type 2 Diabetes, Steroid-induced Diabetes
In brief
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.
Key facts
- Study ID
- NCT07510386
- Run by
- Icahn School of Medicine at Mount Sinai
- People needed
- 64
- Starts
- 2026-09-30
- Expected to finish
- 2026-11-01
- Last updated by the study team
- 2026-08-10
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult 18 years or older.
- Inpatient treatment for type 2 or steroid induced diabetes during hospitalization, with plan for insulin use after discharge.
You may not qualify if…
- Type 1 diabetes
- Plan for discharge to rehabilitation/skilled nursing/hospice facility
- Contra-indication to sensor placement
- Pregnancy
Where it is running
- Icahn School of Medicine at Mount Sinai — New York, New York, United States
Full record on ClinicalTrials.gov
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