Status:
ACTIVE_NOT_RECRUITING
AV-23-001 AVAVA MIRIA Pilot Study
Lead Sponsor:
AVAVA, Inc.
Conditions:
Wrinkle
Acne Scars - Mixed Atrophic and Hypertrophic
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This non-significant risk study is intended to demonstrate the use of the MIRIA Skin Treatment System can show improvement in dermatologic conditions currently indicated for treatment with a laser (su...
Detailed Description
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 condi...
Eligibility Criteria
Inclusion
- 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
- 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.
Key Trial Info
Start Date :
November 6 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2026
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT06557434
Start Date
November 6 2023
End Date
December 31 2026
Last Update
March 7 2025
Active Locations (2)
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1
Skinfluence Long Island
Dix Hills, New York, United States, 11746
2
Laser and Skin Surgery Center of New York
New York, New York, United States, 10010