Hybrid Fractional Laser for Treatment of Off Face Body Skin Quality

Completed · Not applicable

Conditions studied: Skin Laxity

In brief

To demonstrate effectiveness of hybrid fractional laser for the treatment of poor skin quality on the decolletage, back of the hands and lower legs

Key facts

Study ID

NCT03969485

Run by

Sciton

People needed

7

Starts

2019-04-29

Expected to finish

2020-10-12

Last updated by the study team

2020-10-20

Who can join

Age: 40 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy male/female subjects between 40 to 65 years of age inclusive
• Fitzpatrick skin type I-III
• Non-smokers or have not smoked (including vaping) within the past 14 days from the screening visit
• Has poor skin texture
• Has mild thin skin
• Has some level of dyschromia on the treatment area as assessed by the Investigator
• Can read, understand and sign informed consent form (English only)
• Has indicated willingness to participate in the study by signing an informed consent form
• Agrees to adhere to the treatment and follow-up schedule and post treatment care instructions

You may not qualify if…

• Fitzpatrick skin type IV-VI
• Has tanned within the past 30 days or is unable or unlikely to refrain from tanning, including the use of tanning booths, tanning spray or cream
• Has tattoos, dysplastic nevi on the treatment area
• Is pregnant and/or lactating
• History or current photosensitivity
• History or current use of medication with photosensitizing properties within past 6 months
• History or current of chronic reoccurring skin disease or disorder affecting treatment area
• History or current cancer of any type
• Has signs of actinic bronzing
• Has open lacerations, and abrasions on the treatment area
• History of keloid formation, or hypertrophic scar formation, or poor wound healing
• History of bleeding disorder, or is currently taking anticoagulation medications
• Has significant concurrent illnesses (controlled or uncontrolled), such as diabetes, lupus, epilepsy, or cardiac disorders, which might be aggravated as a result of treatment
• Has participated in any clinical trial involving an investigational drug, device or cosmetic product or procedure within the past 30 days
• The investigator feels that for any reason the subject is not eligible to participate in the study

Where it is running

• New Jersey Clinical Research Center — Montclair, New Jersey, United States

Full record on ClinicalTrials.gov

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