Evaluation of the Dermal Cooling System for the Enhanced Treatment of Benign Pigmented Lesions and Common Skin Conditions

R2 Dermatology

Status

Completed

Conditions

Pigmentation

Treatments

Device: Dermal Cooling System

Study type

Interventional

Funder types

Industry

Identifiers

NCT04493021

R2-20-001

Details and patient eligibility

About

The purpose of this study is to evaluate the Dermal Cooling System for lightening of benign pigmented lesions and to assess additional cosmetic benefits.

Full description

This is a prospective, non-randomized, open-label study to evaluate the effectiveness of the Dermal Cooling system to reduce pigmentation in benign pigmented lesions and to determine if additional cosmetic benefits are achieved.

Enrollment

137 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Male or female subjects > 18 years of age.
Subject has one or more benign pigmented lesions (e.g., solar lentigines, freckles, seborrheic keratosis), in an area suitable for treatment.
Subject is willing to have up to 40 treatment sites treated per treatment session depending on the size and nature of the lesions identified.
Subject is willing to have digital photographs taken of the treatment area and agrees to use of photographs for presentation, educational, or marketing purposes.
Subject is willing to cover treated area or have very limited sun exposure and use an approved sunscreen of SPF 50 or higher on the treated area for the duration of the study, including the follow-up period, if requested.
Subject has read and signed a written informed consent form.
Subject is willing to comply with adjuvant topical regimen, as applicable. -

Exclusion criteria

Physician prescribed medical or surgical treatment, or use of over-the-counter products to alter skin color, in the area of intended treatment in the previous 6 months (e.g., hydroquinone, corticosteroids, laser surgery)
Use of products containing glycolic acids, retinol, salicylic acid within the previous 2 weeks
Use of Accutane within the previous 6 months
Artificial tanning in the area of intended treatment within 1 month (e.g., spray, lotion, tanning bed) or intention to use artificial tanning within the follow-up period
Scars or tattoos in the location of the treatment sites
History of melasma, vitiligo, eczema, or psoriasis in the area of treatment
History of melanoma
Subject is pregnant or intending to become pregnant during the study period
Subject is lactating or has been lactating in the past 6 months
Known history of illness or adverse reaction to cold insult (e.g., cryoglobulinemia, cold urticaria, paroxysmal cold hemoglobinuria, Reynaud's disease.
History of abnormal wound healing or abnormal scarring
Inability or unwillingness to comply with the study requirements.
Current enrollment in a clinical study of any other unapproved investigational drug or device.
Any other condition or laboratory value that would, in the professional opinion of the investigator, potentially affect response or participation in this clinical study, or would pose an unacceptable risk to the subject.