Study of Picosecond and Nanosecond Q-switched Lasers for Tattoo Removal

NCT ID: NCT01973166

Last Updated: 2023-02-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 42 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-09-30
• Study Completion Date: 2014-07-31

Brief Summary

The purpose of this study is to compare the investigational medical grade laser device to a marketed medical grade laser device for effectiveness in lightening or clearing unwanted tattoos. This study will also compare any side effects from treatment with the devices.

Detailed Description

This is a two center study to evaluate the Cutera RF system. Subjects will be treated on the abdomen and / or flanks areas and / or saddle bag (upper lateral thigh, lateral hip and lower buttocks).

The objective of this study is to evaluate the thermal and histological changes observed in the subcutaneous tissue following RF exposure.

Conditions

Tattoo Removal

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Picosecond Q-switched Laser Treatment

Picosecond Q-switched Nd:YAG (1064 nm and 532 nm) laser

Group Type: EXPERIMENTAL

Picosecond Q-switched Laser Treatment

Intervention Type: DEVICE

Nanosecond Q-switched Laser Treatment

Nanosecond Q-switched Nd:YAG (1064 nm and 532 nm) laser

Group Type: ACTIVE_COMPARATOR

Nanosecond Q-switched Laser Treatment

Intervention Type: DEVICE

Interventions

Picosecond Q-switched Laser Treatment

Intervention Type: DEVICE

Nanosecond Q-switched Laser Treatment

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Females or Males, 18 to 65 years of age (inclusive)
• Fitzpatrick Skin Type I - IV (Appendix 3)
• Tattoos containing black/blue ink alone or in combination with other colors
• Target tattoos older than 1 year
• Presence of tattoos equal or greater than 2 square inches, not to exceed 12 square inches
• 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 use hydroquinone approximately 4 weeks pre-treatment and post- treatment if required
• Willingness to have digital photographs taken of the treated area
• Agree not to undergo any other procedure(s) for the tattoo removal during the study
• 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

Exclusion Criteria

• Participation in a study of another device or drug within 6 months prior to enrollment or during the study
• Prior treatment for tattoo removal in the target area, e.g., with q-switched laser, IPL, dermabrasion, electrocautery, cryotherapy
• History of allergic reaction to pigments following tattooing
• Presence of double tattoo in the treatment area
• 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, such as tetracycline
• History of herpes simplex and/or herpes zoster (shingles)
• 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 within 12 months of study participation
• Use of oral isotretinoin within 12 months of study participation and topical use of isotretinoin within 6 months on the treated area
• Anytime in life, having have 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
• As per the Investigator's discretion, any physical or mental condition which might make it unsafe for the subject to participate in this study

• 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

David Apfelberg

Role: PRINCIPAL_INVESTIGATOR

Study Principal Investigator

Locations

Brisbane, California, United States

Countries

United States

Other Identifiers

C-13-TPS04

Identifier Type: -

Identifier Source: org_study_id