Evaluating full-body imaging technology for skin disease detection
Official title: DermaFlow Alpha - Multi-modal Quantitative Imaging of the Skin
Run by HJN Sverige AB/Neko Health · NCT06989216 · Data updated 2026-11-12
This study is testing a new full-body imaging technology to see if it can help doctors better detect and monitor skin diseases like skin cancer and eczema.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 8000 (estimated) |
| Sponsor | HJN Sverige AB/Neko Health Industry-sponsored |
| Locations | 3 sites (Stockholm and 2 other locations) |
| Status | Recruiting |
| Started | February 1, 2023 |
| Main results expected | February 1, 2026 |
| Study ends | February 1, 2026 |
| Registry record updated | May 25, 2025 |
| Trial ID | NCT06989216 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adult patients visiting primary care facilities who can provide informed consent.
✕Probably not a fit
Patients with cognitive impairments or severe disorders may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical investigation assesses the feasibility of using full-body multi-modal imaging technology for screening and monitoring various skin diseases, including skin cancer and atopic dermatitis. Participants undergo a primary care visit where high-resolution 2D and 3D images, along with thermal images, are captured to evaluate skin lesions. The study aims to correlate these imaging results with clinical diagnoses and improve early detection methods in primary care settings.
Why it matters
Potential benefit: If successful, this approach could enhance early detection and monitoring of skin diseases, leading to better patient outcomes.
How similar studies have gone: While the use of multi-modal imaging is gaining traction, this specific approach is relatively novel and has not been extensively tested in similar studies.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion criteria: * Adult patients that are part of the regular healthcare patient flow at the investigational sites, or as separately invited to participate in this investigation. * Patients with signed informed consent Exclusion criteria: * Cognitive impairment * Patients unable to understand the oral and written study information in Swedish or English * Other severe disorder or terminal disease * Patients unable to provide an informed consent * Patients not able to keep balance, while standing up with closed eyes, without any aid * Claustrophobic patients
Where it's running
-
Atrium Health Care Centre
Stockholm, Sweden Recruiting -
Neko Health Centre Regeringsgatan
Stockholm, Sweden Recruiting -
Neko Health Centre Sibyllegatan
Stockholm, Sweden Recruiting
Study contacts
- Principal investigator: Andreea Valdman, MD — Neko Health AB
- Study coordinator: Mattias Windå, MSc
- Email: mattias@nekohealth.com
- Phone: 0703169040
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.