Effect of 2-Week Continuous Glucose Monitoring on Glycemic Management in Patients New-to-Insulin on Hospital Discharge

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: f
View:

• 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- December 31, 2026

• New initiation of insulin therapy, including basal insulin regimen, basal-bolus insulin regimen, or mixed insulin regimen at the time of hospital discharge

Locations
United States
New York
NYU Langone Hospital - Long Island
RECRUITING
Mineola
Contact Information
Primary
Michael Goldstein
Michael.Goldstein@nyulangone.org
516-663-3511
Time Frame
Start Date: 2024-12-16
Estimated Completion Date: 2027-04-30
Participants
Target number of participants: 150
Treatments
Experimental: Continuous Glucose Monitoring (CGM)
Patients in the CGM group will be instructed to wear a CGM uninterruptedly for 2 weeks duration.
Active_comparator: Blood Glucose Monitoring (BGM)
Patients in the BGM group will be instructed to check their blood glucose utilizing fingerstick glucose monitoring multiple times daily depending on their insulin regimen for 2 weeks duration.
Related Therapeutic Areas
Sponsors
Leads: NYU Langone Health

This content was sourced from clinicaltrials.gov