AV-23-001 AVAVA MIRIA Pilot Study

This study is intended to allow clinical evaluation of the feasibility of the MIRIA Skin Treatment System, referred to herein as the SR Skin Rejuvenation Laser, for the treatment of dermatologic conditions currently indicated for treatment with a laser (such as, but not limited to, benign pigmented lesions, benign cutaneous lesions, wrinkles, textural irregularities, or scars). This clinical evaluation is being performed under an investigational protocol to formally collect data for the treatment of different dermatologic conditions.

This prospective, non-randomized, controlled study will include subjects with dermatologic conditions that are currently indicated for treatment with a laser who are willing to have sites exposed to the MIRIA Laser and who agree to comply with the study requirements during the follow-up period, a minimum of 3 months and a maximum of 18 months. Some areas with the dermatologic condition may be left as a control for the treated section. Subjects may also be directed to use some topical cream or lotion for up to 1 month prior to the laser procedure or during the duration of the study, according to the Investigator's standard practice.

Inclusion criteria

• Male or female subjects > 18 years of age.
• Dermatologic condition currently indicated for laser treatment OR the subject is to be enrolled for assessment of treatment parameters on normal skin.
• Willingness to have multiple areas exposed.
• Willingness to have digital photographs taken of treatment area(s) and agreement with use of photographs for presentation, educational, or marketing purposes.
• Willingness to comply with the following during the study, including the follow-up period:

• maintain consistent skin care regimen on treated areas.
• Willingness to cover treated areas or have very limited sun exposure and, if requested, use an approved sunscreen of SPF 50 or higher.
• refrain from using systemic corticosteroids, according to Investigator discretion.
• refrain from using topical corticosteroids, retinoids, or prescription skin-lightening medications on the treated areas, according to Investigator discretion.
• refrain from any other procedures in the treatment areas.
• Willingness and ability to comply with study instructions and return for required visits.
• Subject understands that fees will be collected at the time of treatment ranging from $300 to $3000 per treatment depending upon number of anatomical areas treated. The exact amount will be disclosed and recorded within the consent.
• Subject has read and signed a written informed consent form.
• Subject lives within 50 miles of study site.
• For Males: Willingness to shave facial hair on treatment areas.

Exclusion criteria

• Skin pathology or condition that could interfere with evaluation of the study procedure, e.g.,
• Systemic treatment prescribed within previous 6 months (e.g., oral medication such as isotretinoin)
• Surgical treatment in the target areas within previous 6 months (e.g., laser surgery)
• Active vitiligo, psoriasis, or eczema in the treatment area
• The timing of use of fillers, neuromodulators and other cosmetic procedures are at the discretion of the investigator.
• Topical treatment applied to target areas within the previous 1 month or according to Investigator discretion.
• Active suntan and unable or unlikely to refrain from tanning within the follow-up period.
• Artificial tanning in the target areas within the previous 1 month (e.g., spray, lotion, tanning bed) or intention to use artificial tanning within the follow-up period.
• Active localized or systemic infection, or an open wound in area being treated.
• Lesions in the treatment areas suspicious for malignancy (skin cancer, melanoma)
• History of abnormal wound healing or abnormal scarring (e.g., hypertrophic or keloid)
• History of connective tissue disease, such as lupus or scleroderma.
• Any use of medication that is known to increase sensitivity to light according to Investigator's discretion (e.g., topicals that produce sensitivity to light may be used in areas other than the target area).
• History of gold therapy.
• History of disease stimulated by heat, such as recurrent herpes simplex or herpes zoster (shingles) in the treatment area, unless treatment is conducted following a prophylactic regimen.
• History of radiation to the treatment area or currently undergoing systemic chemotherapy for the treatment of cancer.
• For Female: Pregnancy or lactation, or intent to become pregnant within the study period.
• Significant uncontrolled concurrent illness, such as diabetes mellitus or cardiovascular disease, e.g., uncontrolled hypertension.
• History of immunosuppression/immune deficiency disorder or currently using immunosuppressive medications.
• Current enrollment in a clinical study of any other unapproved investigational drug or device unless it is a noninvasive dermal study for which the subject is in a follow-up period and has other areas of skin that meet the study criteria or has received an investigational drug or been treated with an investigational device within 30 days prior to entering this study.
• 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.