Use of Electrical Impedance Spectroscopy (EIS) for Early Diagnosis of Skin Damage (DermaSense)

Aristotle University Of Thessaloniki

Status

Terminated

Conditions

Dysplastic Nevus Syndrome

Lichen Planus-Like Keratosis

Squamous Cell Carcinoma

Lentigo Maligna

Melanoma (Skin)

Carcinosarcoma

Seborrheic Keratosis

Basal Cell Carcinoma

Treatments

Diagnostic Test: Electrical Impedence Spectroscopy DermaSense

Study type

Observational

Funder types

Other

Identifiers

NCT04688749

489

Details and patient eligibility

About

The purpose of this clinical study is to evaluate if the DermaSense prototype EIS scanner can provide medical decision support which can complement dermoscopy-based identification of the disease at time of biopsy decision.

Full description

This is a clinical study designed to evaluate if the DermaSense device can be a system of an automated analysis and classification of skin lesions aiming to provide a comprehensive, reliable and cost-effective approach to assist the Dermatologists' decision (biopsy, dermoscopy, histopathological analysis etc). The study enrollment will continue until a minimum of 180 subjects are enrolled in the study. Second Department of Dermatology, School of Medicine, Faculty of Health Sciences of the Aristotle University of Thessaloniki, at the "Papageorgiou" General Hospital will participate in this study. Dermatologists participating in the study will perform the patient and lesion assessment for biopsy as standard of care at the clinic.

EIS (electrical impedance spectroscopy) measurements will be done once per participant recommended by the Dermatologist based on their clinical interest in various areas of the skin. Two sets of measurements will be performed for each participant, either at a nevus in contrast with a nearby clear patch of skin, or at a skin damage area (melanoma, basal cell carcinoma (BCC), squamous cell carcinoma (SCC), etc) in contrast with a nearby clear patch of skin. Also, more repeated measurements may be needed to determine the validity of the measurement result. Evaluation and analysis of the measurement data will be done by the DermaSense team and will be used not only for applying appropriate statistical correlations compared to established dermatological diagnostic methods (eg dermοscopy, histopathological examinations, biopsies etc.) but also for training in artificial intelligence and machine learning methods. Finally, the participants will sign a consent form that is consistent with bioethical rules and according with EU GDPR regulation to protect their personal data.

Enrollment

50 patients

Sex

All

Ages

8 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

The inclusion criteria for patients in this study are as follows:

Male or female at least 8 years old
Individuals diagnosed with confirmed skin damage by Dermatologists
Lesions that present with unclear clinical presentation to allow for clinical diagnosis of benign or minimally dysplastic nevus (nevi), so necessitating a biopsy.
The inclusion of patients in this study is independent from the current therapy. During the study all patients will be kept on a therapy that is medically indicated
Participant himself or legal guardian/representative willing and consenting to participate to the study by giving written informed consent
Participants under 18 years old must have a parent, or / and other reliable caregiver who agrees to accompany him/her to the measurements, provide information about the participant as required by the protocol

The inclusion criteria for healthy controls in this study are as follows:

Male or female at least 8 years old
Matched healthy control population: Individuals without skin damage (melanoma, BCC, SCC, etc) that have been included in cohort.
Lesions that present with unclear clinical presentation to allow for clinical diagnosis of benign or minimally dysplastic nevus (nevi), so necessitating a biopsy.
The inclusion of patients in this study is independent from the current therapy. During the study all patients will be kept on a therapy that is medically indicated
Participant himself or legal guardian/representative willing and consenting to participate to the study by giving written informed consent
Participants under 18 years old must have a parent, or / and other reliable caregiver who agrees to accompany him/her to the measurements, provide information about the participant as required by the protocol

Exclusion Criteria:

concurrent participation in another relevant study
occurrence of skin damage during the study
Subjects who fail to provide informed consent
Study subjects with underlying medical disease which may alter ability to diagnose clinically or inhibit DermaSense prototype EIS scanner from collecting data