Actively Recruiting
DermaFlow Alpha Multi-modal Quantitative Imaging of the Skin for Screening and Diagnosis in Primary Care
Led by HJN Sverige AB/Neko Health · Updated on 2025-05-25
8000
Participants Needed
3
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the use of a full-body multi-modal imaging technology to help with screening, monitoring, and diagnosing various skin and circulatory conditions in primary care. This study focuses on assessing the accuracy of body measurements and the technology's ability to detect skin cancer, peripheral arterial disease, Raynaud's phenomenon, and other dermatological conditions. The imaging system combines high-resolution 2D and 3D color photos with thermal images to capture detailed information about skin lesions and microcirculation. The imaging technology uses camera systems that include 2D color cameras for capturing lesion appearance, 3D cameras for geometric alignment and measurements, and thermal cameras for detecting temperature changes linked to skin and vascular diseases. Participants will have full-body images taken from the front and back during their primary care visit. Some participants may also have manual body measurements taken as part of routine care. Those interested may have repeated image and measurement sessions yearly. Participants will fill out a questionnaire about their medical history related to the studied conditions during the visit. Researchers will evaluate the sensitivity of the imaging for detecting lesions needing removal, dermatological conditions, and changes in lesions compared to visual inspection and traditional measurements. Thermal gradients will be analyzed for correlations with peripheral arterial disease and Raynaud's phenomenon. Follow-up assessments may occur at one year. The study offers a non-invasive way to collect detailed skin and body data with ongoing safety and diagnostic monitoring.
CONDITIONS
Brief Title
Multi-modal Quantitative Imaging of the Skin
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients who are part of regular healthcare at the investigational sites or invited separately
- Patients who have signed informed consent
You will not qualify if you...
- Cognitive impairment
- Unable to understand oral and written study information in Swedish or English
- Presence of other severe disorders or terminal disease
- Unable to provide informed consent
- Unable to stand with eyes closed without aid
- Claustrophobic patients
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 1 day
Participants undergo full-body multi-modal imaging including 2D and 3D color images and thermal images to assess skin conditions and body measurements. They also complete a questionnaire on-site about their skin and related diseases.
1 visit (in-person)
Duration - Up to several years
Participants may have repeated yearly imaging and assessments to monitor skin conditions and body metrics over time.
Annual visits depending on participant interest
Trial Site Locations
Total: 3 locations
1
Atrium Health Care Centre
Stockholm, Sweden
Actively Recruiting
2
Neko Health Centre Regeringsgatan
Stockholm, Sweden
Actively Recruiting
3
Neko Health Centre Sibyllegatan
Stockholm, Sweden
Actively Recruiting
Research Team
M
Mattias Windå, MSc
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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