Efficacy and Safety of PiQo4 Device for Treatment of Melasma

Focus Medical

Status

Completed

Conditions

Melasma

Treatments

Device: PiQo4

Study type

Interventional

Funder types

Industry

Identifiers

NCT03565341

Focus-PiQo4 Melasma-17-04

Details and patient eligibility

About

Single center, Prospective, Open Label with Split-face Study Design. Face sides will be randomized to receive either 1064nm alone or 1064nm & 585nm combination treatment.

Each subject will receive up to 3 treatments at monthly intervals (±4 days). Follow-up visits will take place at 1, 3, and 6 months following the last treatment.

Enrollment

20 patients

Sex

Female

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Healthy Female
Age= 18-75.
Fitzpatrick skin phototype = II-V
Melasma severity: diagnosed with mild to severe melasma lesions (MSS≥2)
Melasma type: Dermal or mixed type melasma, confirmed by Wood's lamp test
Melasma duration: The subject's melasma has persisted for greater than 6 months
Melasma previous treatments: has failed to respond to conventional treatment with hydroquinone or other topical lightening agents
Able to read, understand and provide written Informed Consent.
Able and willing to comply with the treatment/follow-up schedule and post treatment care
Agreed to use the same facial skin care products during the clinical trial period (including the follow-up period)
Agreed to the prohibition of the use of local/systemic corticosteroids or retinoids and other local/systemic lightening medications, and willing to abide by such instructions
Agreed to the daily use of an over SPF 50 sunblock on their face during the clinical trial period (including the follow-up period), and willing to abide by such instructions
Agreed to have their face photographed and willingness to allow Focus Medical (the study Sponsor) and Lumenis and the investigators to use de-identified photographs of the treated area for presentation and publication purposes
(In case of fertile women) Tested negative in the pregnancy test and agreed to use birth control contraceptives during the clinical trial period - Oral contraceptives are forbidden as they may influence the results of the clinical study.
Agreed not to undergo any other procedure on their face during their participation in the clinical trial

Exclusion criteria

Pregnant, intending to become pregnant during the course of study, less than 3 months postpartum or less than 3 months after completion of breastfeeding
Known hypersensitivity or contraindications to anaesthetic agents including lidocaine and its derivatives
Participation in a study of another device or drug within three months prior to enrolment or during the study.
Presence of open wounds or lesions in the area
Extensive scarring or tattoos in areas to be treated.
Having other pigmentation disorder
Having an excessive underlying vascular condition (e.g. dense network of capillaries).
Suffering from current or history of significant skin conditions in the treated area that could interfere with the evaluation (i.e. infection, dermatitis, or rash on their face) or requires the use of interfering topical or systemic therapy.
Excessively tanned in areas to be treated or unable/unlikely to refrain from tanning during the study.
Having a history of diseases stimulated by heat, such as recurrent Herpes Simplex in the treated area, unless treatment is conducted following a prophylactic regimen
Subjects who are opposed to possible damage to the hair follicles with possible loss of hair in the treatment area
Laser or medium/deep chemical peel, or surgery, or filler treatments using collagen, hyaluronic acid, or any other material at area of treatment, within 6 months of initial treatment or during the course of the study.
IPL or superﬁcial chemical peel within the previous 1 month
Topical therapy with retinoids, imiquimod, 5-ﬂuorouracil, ingenol mebutate, diclofenac, alpha-hydroxy acids, or salicylic acids within the previous 1 month.
Currently using topical retinoid, hydroquinone or corticosteroid or whitening cream such as alpha arbutin, azelaic acid, kojic acid ascorbic acid or any cosmetics within 2 weeks
Lightening oral medication (hydroquinone, tranexamic acid), isotretinoid (or retinoid), light-sensitive medication, or steroids in the last 6 months
History of keloid scarring, hypertrophic scarring, or of abnormal wound healing.
History of connective tissue diseases such as systemic lupus erythematosus or scleroderma
Active leukoplakia, eczema, or psoriasis in the treatment area
History of post inflammatory pigmentary disorders, particularly a tendency for hyper- or hypo-pigmentation.
History of cutaneous photosensitization, porphyria, and hypersensitivity to porphyrins or photodermatosis.
Has used photosensitizing drugs (e.g., Declomycin, sulfa antibiotics, phenothiazines, etc.) within a timeframe where photosensitization from these drugs may still be present
History of skin cancer in the treatment area
Significant concurrent illness or any disease state that in the opinion of the Investigator would interfere with the treatment or healing process
History of immunosuppression/immune deficiency disorders (including HIV infection or AIDS) or currently using immunosuppressive medications.
Having a known anticoagulative or thromboembolic condition or taking anticoagulation medications one week prior to and during the treatment course (to allow inclusion, temporary cessation of use as per the subject's physician's discretion).
History of hormonal therapy in the last 3 months (e.g., estrogen, progesterone, or oral contraceptive)
As per the Investigator's discretion, any physical or mental condition which might make it unsafe for the subject to participate in this study