Actively Recruiting
Improving Glycemic Control With Telemedicine and Smart Insulin Pens
Led by University of Maryland, Baltimore · Updated on 2026-02-10
50
Participants Needed
2
Research Sites
121 weeks
Total Duration
On this page
Sponsors
U
University of Maryland, Baltimore
Lead Sponsor
M
Medtronic
Collaborating Sponsor
AI-Summary
What this Trial Is About
Almost 40% of veterans have diabetes, the proposed research may improve clinical care among veterans with diabetes. In this application we are going to examine whether utilizing Smart Insulin pens (SIPs) with CGMs and telemedicine is a better tool for managing diabetes compared to traditional insulin pens, CGMs and telemedicine, leading to improved blood sugar control and better clinical outcomes.
CONDITIONS
Official Title
Improving Glycemic Control With Telemedicine and Smart Insulin Pens
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age or older
- Receiving multiple daily insulin injections (MDI) for at least 3 months before the study
You will not qualify if you...
- Not treated with MDI for at least 3 months (includes diet only, non-insulin medications only, basal insulin only, or short-acting insulin only)
- Using insulin pumps at screening
- Pregnant patients
- Extensive skin disease or allergies preventing use of CGM sensor
- End-stage renal disease requiring dialysis
- Significant psychiatric illness or inability to understand study
- Receiving hydroxyurea or chronic acetaminophen treatment
- Started or changed dose of non-insulin diabetes medications within 60 days before study
- No access to a compatible smartphone for digital health applications
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Baltimore VA Maryland Center
Baltimore, Maryland, United States, 21201
Actively Recruiting
2
VAMHCS, Diabetes Outpatient Clinic
Baltimore, Maryland, United States, 21201
Not Yet Recruiting
Research Team
W
William Scott, MS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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