Ireland
--:--IST
Recruiting Not applicable

Application of the Belle.AI Dermatological Image Reference System for Patient Diagnosis in an Active Clinical Setting

NCT06724627 · tracked via the Priya Life Science USA tracker
Sponsor
BelleTorus Corporation
Phase
Not applicable
Started
2024-09-16
Last updated
2024-12-09

Condition(s) studied

Skin ConditionDermatologyDermatology/Skin - Other

Investigational drug(s) / intervention(s)

Dermatology/Skin - Other

Dermatology/Skin - Other: Belle AI for skin image assessment.

Study summary

The goal of this research study is to test a new, investigational tool that uses artificial intelligence (AI) to help primary care providers assess skin conditions. This tool is an AI-powered dermatology image reference app that works with a smartphone. For clarity, the AI makes no diagnoses; it provides reference images. Primary care providers then use their own medical judgement and training to make the diagnosis.

The sponsor aims to compare the diagnoses made by primary care providers (such as doctors, nurse practitioners, and physician assistants) with the support of the AI tool compared to a panel of dermatologists, who are setting the gold standard. By doing so, the sponsor can determine the value of the AI tool for primary care providers and understand how it might be used alongside traditional clinical care.

This AI capability complies with FDA regulatory guidelines and is not considered a medical device, similar to a Google image search, which returns similar looking images for reference purposes. For intervention, they healthcare providers use their own training and clinical judgement to make the diagnosis, and not the AI.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient must present to walk-in clinic with a primary dermatological complaint. * Patient must have the ability and willingness to provide informed consent and comply with study procedures and visits. * Participants must have access to the required technology (e.g., smartphone with internet access) and be capable of using it for the required image capture. Exclusion Criteria: * Patients who are unable to comply with study procedures due to physical or mental health limitations (as assessed by study coordinator). * Pediatric, adolescent, and teen patients who present with dermatological conditions on their genitalia will not be included in the study (in support of patient privacy concerns).

Primary outcome measure(s)

  • Accuracy of Belle AI Image References — Through study completion, an average of 14 days
    Comparison of Belle AI's image reference system primary probability diagnosis to the reference diagnosis established by the dermatological review committee; additional evaluation of the accuracy of the second and third highest probability diagnoses determined by the Bell Image Match Score
  • Impact on Economic Burden — Through study completion, an average of 14 days
    Measure economic impact by enabling remote assessment for patients

Trial sites (1)

FacilityCityRegionStatus
Urban Health Plan Inc. The Bronx New York Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06724627 on ClinicalTrials.gov ↗ ← All trials in the USA