Actively Recruiting
The Skin Barrier in Users of Diabetes Devices
Led by Jannet Svensson · Updated on 2025-09-09
150
Participants Needed
1
Research Sites
94 weeks
Total Duration
On this page
Sponsors
J
Jannet Svensson
Lead Sponsor
L
Linkoeping University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Diabetes technology (insulin pumps and continuous glucose monitoring) have become standard of care in children with type 1 diabetes. Unfortunately, the attachment of the devices to the skin can provoke injury, irritative or allergic eczema of the skin. Additionally, the continuous insulin infusion often causes sub-cutaneous lipohypertrophy. These occurrences are likely to increase blood glucose fluctuation and impact burden of diabetes. In collaboration with dermatologists, the propose is to investigate the skin microcirculation and skin barrier as well as the subcutaneous tissue when exposed to insulin, occlusion, irritative and allergenic features of the part of device in close contact with the skin. Secondly, investigate the skin barrier and recovery time as a function of time since exposure, type of patches/device and use of preventive strategies like steroids, liquid barrier crème or local anesthetic. To study microcirculation the investgators use Tissue Viability Imaging (TiVI) a non-invasive method using polarization light spectroscopy to count red blood cells thereby saying something about the microcirculation. To investigate skin barrier, the investigators use electric impedance spectroscopy (EIS) which is a non-invasive method sending small electric current of different frequencies through the skin surface. The different frequencies have different properties regarding penetration of cells making it possible to measure the resistance towards each frequency. In this way give a measure of the skin barrier. The last methods investigators are using is ultrasound a non-invasive method that uses sound to show different structures in the subcutaneous tissue, it has been demonstrated to be better than visual inspection to detect lipohypertrophy in the subcutaneous tissue. Lipohypertrophy is often seen in places with repeated infusion/injection of insulin. These investigations are necessary to motivate and guide the development of new materials for diabetes devices and provide clinical guidelines regarding device position and site rotation in order to prevent skin complications from interfering with optimal treatment. This could lead to improved short and long-term outcome in the care of persons with diabetes.
CONDITIONS
Official Title
The Skin Barrier in Users of Diabetes Devices
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with type 1 diabetes
- Currently using a diabetes device attached to the skin (insulin pump or continuous glucose monitor)
- Age between 2 and 17 years
- Able to understand and communicate in Swedish or English
You will not qualify if you...
- Not using a diabetes device attached to the skin
- Unable to read and understand Swedish or English
- Cognitive impairment that affects ability to answer questionnaires or participate in phone follow-ups
AI-Screening
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Trial Site Locations
Total: 1 location
1
Crown Princess Victoria Children´s Hospital
Linköping, Sweden, 58185
Actively Recruiting
Research Team
J
Jannet Svensson, PhD
CONTACT
P
Pär A White, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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