Pilot Study of Multi-wavelength Laser for Tattoo Removal

NCT ID: NCT03290547

Last Updated: 2023-09-15

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 22 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-07-08
• Study Completion Date: 2017-11-29

Brief Summary

To evaluate the safety and efficacy of an investigational version of the Cutera enLighten laser that offers muliple wavelengths for tattoo removal.

Detailed Description

Currently, the enLighten laser offers two wavelengths: 532nm and 1064nm. The version of the laser under investigation allows the user to choose a wavelength between 640nm to 800nm.

This is a multi-center prospective, open-label, uncontrolled pilot study in up to 75 male or female subjects, age 18 to 65 years, who desire laser removal of a tattoo containing single or multi-color ink. Subjects will receive laser treatments and will be followed at 6 weeks.

Conditions

Tattoo Removal

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

arm-1

Cutera enLighten laser treatments that allows the user to choose a wavelength between 640nm to 800nm.

Group Type: OTHER

Cutera enLighten laser

Intervention Type: DEVICE

Subjects will receive laser treatments.

Interventions

Cutera enLighten laser

Subjects will receive laser treatments.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Female or Male, 18 to 65 years of age (inclusive).

2. Fitzpatrick Skin Type I - VI (Appendix 3).

3. Target tattoo contains single or multi-color ink.

4. Subject must be able to read, understand and sign the Informed Consent Form.

5. Must be willing and able to adhere to the treatment and follow-up schedule and post-treatment care instructions.

6. 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.

7. Willing to have digital photographs taken of the treatment area and agree to use of photographs for presentation, educational or marketing purposes.

8. Agree to not undergo any other procedure(s) for tattoo removal during the study (as applicable).

9. 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.

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Exclusion Criteria

1. Participation in a clinical trial of a drug or another device in the target area during the study..

2. Target tattoo contains only black ink.

3. History of allergic reaction to pigments following tattooing..

4. History of allergy to local anesthetics.

5. History of allergy to topical antibiotics.

6. History of malignant tumors in the target area.

7. Skin abnormalities in the target area, e.g., cuts, scrapes, wounds, scars, large moles.

8. Pregnant and/or breastfeeding.

9. Having an infection, dermatitis or a rash in the treatment area.

10. Significant concurrent illness, such as diabetes mellitus or cardiovascular disease, e.g., uncontrolled hypertension.

11. Suffering from coagulation disorders or taking prescription anticoagulation medications.

12. History of keloid scarring, hypertrophic scarring or of abnormal wound healing.

13. History of immunosuppression/immune deficiency disorders or currently using immunosuppressive medications.

14. History of vitiligo, eczema, or psoriasis.

15. History of connective tissue disease, such as systemic lupus erythematosus or scleroderma.

16. History of seizure disorders due to light.

17. Any use of medication that is known to increase sensitivity to light according to Investigator's discretion.

18. 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.

19. History of radiation to the treatment area or undergoing systemic chemotherapy for the treatment of cancer.

20. History of pigmentary disorders, particularly tendency for hyper- or hypo-pigmentation.

21. Systemic use of corticosteroid or isotretinoin within 6 months of study participation.

22. Anytime in life, having have used gold therapy (gold salts) for disorders such as rheumatologic disease or lupus.

23. Excessively tanned in areas to be treated or unable/unlikely to refrain from tanning during the study.

24. Current smoker or history of smoking within 6 months of study participation.

25. As per the Investigator's discretion, any physical or mental condition which might make it unsafe for the subject to participate in this study.

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• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Cutera Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Stephen Ronan, M.D.

Role: PRINCIPAL_INVESTIGATOR

Cutera Research Center

Jeffrey Dover, M.D.

Role: PRINCIPAL_INVESTIGATOR

Skin Care Physicians

Locations

Cutera Research Center

Brisbane, California, United States

Skin Care Physicians

Chestnut Hill, Massachusetts, United States

Countries

United States

Provided Documents

Document Type: Study Protocol

View Document

Other Identifiers

C-15-EN10

Identifier Type: -

Identifier Source: org_study_id