A Clinical Evaluation for Tattoo Removal

Stopped early · Not applicable

Conditions studied: Tattoo Removal

In brief

Evaluate safety and efficacy with the enlighten laser for tattoo removal.

Key facts

Study ID: NCT02756806
Run by: Cutera Inc.
People needed: 7
Starts: 2016-04-01
Expected to finish: 2016-09-28
Last updated by the study team: 2023-02-21

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

Female or Male, 18 to 65 years of age (inclusive).
Fitzpatrick Skin Type I - VI (Appendix 3).
Target tattoo contains single or multi-color ink, which includes blue and/or green.
Target tattoos must be older than 1 year.
Target tattoo not to exceed 12 square inches.
Subject must be able to read, understand and sign the Informed Consent Form.
Must be willing and able to adhere to the treatment and follow-up schedule and post-treatment care instructions.
Wiling to cover tattoos with a bandage or clothing; and/or have very limited sun exposure and use an approved sunscreen of SPF 50 or higher on the treated area starting 2 to 4 weeks before the treatment and/or every day for the duration of the study, including the follow-up period.
Willing to have digital photographs taken of the treatment area and agree to use of photographs for presentation, educational or marketing purposes.
Agree to not undergo any other procedure(s) for tattoo removal during the study (as applicable).
Post-menopausal or surgically sterilized, or using a medically acceptable form of birth control at least 3 months prior to enrollment and during the entire course of the study, and no plans to become pregnant for the duration of the study.

You may not qualify if…

Participation in a clinical trial of a drug or another device in the target area within 6 months prior to enrollment or during the study.
Target tattoo contains only black ink.
Target tattoo is a double tattoo where a first tattoo was covered with a second tattoo.
History of allergic reaction to pigments following tattooing.
History of allergy to local anesthetics.
History of allergy to topical antibiotics.
History of malignant tumors in the target area.
Skin abnormalities in the target area, e.g., cuts, scrapes, wounds, scars, large moles.
Pregnant and/or breastfeeding.
Having an infection, dermatitis or a rash in the treatment area.
Significant concurrent illness, such as diabetes mellitus or cardiovascular disease, e.g., uncontrolled hypertension.
Suffering from coagulation disorders or taking prescription anticoagulation medications.
History of keloid scarring, hypertrophic scarring or of abnormal wound healing.
History of immunosuppression/immune deficiency disorders or currently using immunosuppressive medications.
History of vitiligo, eczema, or psoriasis.
History of connective tissue disease, such as systemic lupus erythematosus 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.
History of disease stimulated by heat, such as recurrent herpes simplex and/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.
History of pigmentary disorders, particularly tendency for hyper- or hypo-pigmentation.
Systemic use of corticosteroid or isotretinoin within 6 months of study participation.
Anytime in life, having used gold therapy (gold salts) for disorders such as rheumatologic disease or lupus.
Excessively tanned in areas to be treated or unable/unlikely to refrain from tanning during the study.
Current smoker or history of smoking within 6 months of study participation.

Where it is running

Cutera Research Center — Brisbane, California, United States

Full record on ClinicalTrials.gov

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