AVAVA SR-1 Wrinkles and BPL Study

Avava

Status

Completed

Conditions

Benign Pigmented Lesion

Wrinkle

Treatments

Device: SR-1 Laser

Study type

Interventional

Funder types

Industry

Identifiers

NCT04925921

AV-21-003

Details and patient eligibility

About

This study is being conducted to evaluate the safety and efficacy of a laser called the SR-1 Skin Treatment System, or SR-1 Laser, for the treatment of wrinkles and pigmented spots. Participants will be treated with the SR-1 Laser 3 or 4 times with each treatment spaced 4-6 weeks apart. The improvement in wrinkles and pigmented spots will be evaluated 1 and 3 months after the final treatment.

Enrollment

20 patients

Sex

All

Ages

22 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Wrinkles on both sides of the face (e.g., peri-oral, peri-orbital, and cheek) scored 4-9 on the Fitzpatrick Wrinkle and Elastosis Scale
Willingness to have both sides of the face exposed to the SR-1 Laser.
Willingness to have digital photographs taken of their face and agreement with use of photographs, with their identity protected, for presentation, educational, or marketing purposes.
Willingness to comply with the following during the study, including the follow-up period:
1. maintain consistent skin care regimen on treated areas
2. cover treated areas or have very limited sun exposure and use a provided sunscreen as directed by the Investigator
3. refrain from using systemic corticosteroids
4. refrain from using systemic or topical skin-lightening medications or retinoids
5. refrain from any other procedures in the treatment areas
Willingness and ability to comply with study instructions and return for required visits.

Exclusion criteria

Skin pathology or condition, or medication use that could interfere with evaluation of the study procedure, e.g.,
1. Isotretinoin use within previous 6 months
2. Surgical treatment in the target areas within previous 6 months
3. Active vitiligo, psoriasis, or eczema, or history of these in the treatment area
Injection of botulinum toxin in the treatment areas within the previous 3 months.
Facial cosmetic procedures in the target areas within previous 6 months (e.g., laser or other energy-based device treatment, microdermabrasion, microneedling, chemical peel, injection of dermal filler).
Current smoker or history of smoking greater than 0.5 pack/day in past 5 years.
Excessive sun exposure in the previous month, or unable or unlikely to refrain from tanning or excessive sun exposure during the study.
Artificial tanning (e.g., tanning bed or tanning lotion/spray) in the target areas within previous 1 month or intention to use artificial tanning during the study.
Active localized or systemic infection, or an open wound in area being treated.
History of abnormal wound healing or abnormal scarring (e.g., hypertrophic or keloid).
History of connective tissue disease, such as lupus or scleroderma.
History of seizure disorders due to light.
Any use of medication that is known to increase sensitivity to light according to Investigator's discretion (e.g., topicals sensitive to light may be used in other areas off-face).
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 undergoing systemic chemotherapy for the treatment of cancer. Current cancerous lesion in the treatment area.
Pregnancy or lactation, or intent to become pregnant within the study period.
Significant uncontrolled concurrent illness, such as diabetes mellitus, hypertension, or cardiovascular disease.
History of immunosuppression/immune deficiency disorder or currently using immunosuppressive medications.
Planned weight loss of greater than five pounds.
Facial hair in the treatment areas which would prevent evaluation of the outcome measures.
Current enrollment in a clinical study of any other investigational drug or device, or has received an investigational drug or been treated with an investigational device within 6 months prior to entering this study, unless the other clinical study only involves noninvasive imaging.
Any other physical or mental 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.