DERM US and EU Validation Study

NCT ID: NCT05126173

Last Updated: 2023-06-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1111 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-03-15

Study Completion Date

2022-09-15

Brief Summary

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This study aims establish the effectiveness of Image Analysing Algorithm (DERM) to identify melanoma, Squamous Cell Carcinoma (SCC) and Basal Cell Carcinoma (BCC) when used to analyse dermoscopic images of skin lesions within the US and European population.

Detailed Description

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Conditions

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Malignant Skin Melanoma T0 Basal Cell Carcinoma Squamous Cell Carcinoma

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Deep Ensemble for the Recognition of Malignancy (DERM)

An AI-based diagnosis support tool

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Willing and able to give informed consent for participation in the study,
* Male or Female, aged 18 years or above,
* Have at least one suitable skin lesion that will be biopsied due to a suspicion of skin cancer,

To be suitable for inclusion, a skin lesion must NOT have ANY of the following limitations:

located on an anatomical site of different skin structure: palms of hands or soles of feet (acral lesion), mucosal surfaces (lips and eyes) or under nail (ungal lesion), a diameter greater than the diameter of the dermoscopic lenses, located on an anatomical site unsuitable for photographing, including on surface of genitals and hair-bearing areas, has been previously biopsied, excised, treated or otherwise traumatised, located in an area of visible scarring or tattooing.

\- In the Investigator's opinion, able and willing to comply with all study requirements.

Exclusion Criteria

* Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participant at risk because of participation in the study, or may influence the result of the study, or the participant's ability to participate in the study.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Skin Analytics Limited

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Stanford university

Redwood City, California, United States

Site Status

Vista Health Research, LLC

Miami, Florida, United States

Site Status

Dorisca Research Consulting, LLC

Miami, Florida, United States

Site Status

Northwestern University

Chicago, Illinois, United States

Site Status

ALLCUTIS Research, LLC

Beverly, Massachusetts, United States

Site Status

Allcutis Research

Methuen, Massachusetts, United States

Site Status

Universal Dermatology, PLLC

Fairport, New York, United States

Site Status

University of Pittsburgh Medical Center

Pittsburgh, Pennsylvania, United States

Site Status

Alpesh D. Desai, DO, PLLC, a Houston company institution

Houston, Texas, United States

Site Status

University of Utah

Salt Lake City, Utah, United States

Site Status

Universitaria Di Bologna

Bologna, , Italy

Site Status

Dermatology University of Florence

Florence, , Italy

Site Status

Università degli Studi di Modena e Reggio Emilia

Modena, , Italy

Site Status

University of Campania

Napoli, , Italy

Site Status

Università del Piemonte Orientale

Novara, , Italy

Site Status

UOSD Dermatology Oncology

Roma, , Italy

Site Status

Countries

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United States Italy

Other Identifiers

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DERM-006

Identifier Type: -

Identifier Source: org_study_id

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