About this trial
This study evaluates the feasibility and accuracy of an AI-powered mobile platform (NuvanaDx) for early detection of skin cancer, including melanoma, using smartphone-based imaging. The platform is designed to improve access to early diagnosis, reduce waiting times, and support triage into appropriate care pathways.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
None
Disqualifiers
None
Trial population
Study Population Description: Individuals undergoing dermatology evaluation in UK clinics, supplemented by retrospective anonymized image datasets.
Trial design
Ecologic or community
Prospective
Treatments tested in this trial
Smartphone-based AI skin lesion analysis (NuvanaDx platform).
Diagnostic testSmartphone-based AI skin lesion analysis (NuvanaDx platform).
Treatment groups
Trial outcomes
Primary outcomes
Diagnostic Accuracy of AI tool compared with dermatologist-confirmed diagnosis
Diagnostic Accuracy of AI tool compared with dermatologist-confirmed diagnosis Time Frame: Up to 12 months Measure: Sensitivity, specificity, and predictive values
Sponsors and contacts
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Nuvana Healthcare LTD
Lead sponsor
National Institute for Health Research, United Kingdom
Collaborator