Actively Recruiting
Effect of 2-Week Continuous Glucose Monitoring on Glycemic Management in Patients New-to-Insulin on Hospital Discharge
Led by NYU Langone Health · Updated on 2025-10-02
150
Participants Needed
1
Research Sites
123 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The proposed study will be a randomized, prospective, non-blinded study of 120 participants with type 1 or type 2 diabetes that are new-to-insulin on hospital discharge. On hospital discharge, participants will be assigned to either the intervention of wearing a continuous glucose monitor (CGM) for 2 weeks or blood glucose monitoring (BGM) for 2 weeks. They will have a 2-week follow up visit, during which insulin doses will be adjusted as needed, and a 3-month follow-up visit, at which point HbA1c will be measured.
CONDITIONS
Official Title
Effect of 2-Week Continuous Glucose Monitoring on Glycemic Management in Patients New-to-Insulin on Hospital Discharge
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female aged 18-100 years
- Known history of type 1 or type 2 diabetes
- Admitted to NYU Langone Hospital - Long Island between December 16, 2024 and December 31, 2026
- New initiation of insulin therapy at the time of hospital discharge, including basal insulin, basal-bolus insulin, or mixed insulin regimen
You will not qualify if you...
- Prior use of insulin therapy before hospital admission
- Current use of systemic corticosteroids
- Active pregnancy, determined by patient self-reporting; females who become pregnant during the study will be withdrawn
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
NYU Langone Hospital - Long Island
Mineola, New York, United States, 11501
Actively Recruiting
Research Team
M
Michael Goldstein
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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