Lutronic Infini and LaseMD Systems in Combination Treatment

Lutronic

Status

Completed

Conditions

Face and Neck Wrinkles, Texture, Pigmentation

Treatments

Device: Lutronic LaseMD System

Device: Lutronic Infini System

Study type

Interventional

Funder types

Industry

Identifiers

NCT03409965

L17002

Details and patient eligibility

About

This is a prospective, multi-site, non-randomized study evaluating the safety and effectiveness of the Infini and LaseMD Systems for combination treatment in wrinkles, texture, and pigmentation of the face and/or neck.

Full description

Enrolled subjects will receive three (3) face and/or neck treatments provided 30 days apart. During each treatment subjects will receive both Infini and LaseMD treatments. Treatments will be provided according to a protocol-specific treatment protocol in which an Infini treatment will be provided first, followed by a LaseMD treatment. A telephone contact will be completed at 3 days following each treatment to assess for adverse events. One follow-up visit will be conducted at 90 days following the last study treatment. Outcome measures include clinician grading and subject satisfaction post-treatment. Pre-treatment study photographs and D90 study photographs will be obtained.

Enrollment

21 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Male or female, age 18 years and older.
Subject in good health.
Fitzpatrick Skin Type I to VI.
Solar elastosis on the face and/or neck.
Mild to moderate wrinkles of the face and/or neck.
Mild to moderate textural concerns on the face and/or neck.
Sun and/or age-related pigmentation on the face and/or neck.
Understands and accepts the obligation not to undergo any other procedures in the areas to be treated through the follow-up period.
Willingness and ability to comply with protocol requirements, including returning for follow-up visits and abstaining from exclusionary procedures for the duration of the study.
Subjects of childbearing potential must have a negative urine pregnancy test result and must not be lactating at the Screening Visit and be willing and able to use an acceptable method of birth control (e.g. barrier methods used with a spermicidal agent, hormonal methods, IUD, surgical sterilization, abstinence) during the study. Women will not be considered of childbearing potential if one of the following conditions is documented on the medical history:
1. Postmenopausal for at least 12 months prior to study;
2. Without a uterus and/or both ovaries; or
3. Bilateral tubal ligation at least six months prior to study enrollment.
Absence of physical or psychological conditions unacceptable to the investigator.
Willingness to refrain from use of aspirin, Ibuprofen, Naproxen, or any other NSAID prior to each study treatment and chronic use during the entire post-treatment study period. Washout period, if chronic user, for 4 weeks prior to the first treatment. After all study treatments are completed, limited acute NSAID use is allowed, i.e., a maximum of 2-3 doses in any 2-week period, if needed.
Willingness and ability to provide written consent for study-required photography and adherence to photography procedures (i.e., removal of jewelry and makeup).
Willingness and ability to provide written informed consent and HIPAA authorization prior to performance of any study-related procedure.

Exclusion criteria

Presence of an active systemic or local skin disease that may affect wound healing.
History of keloids or poor wound healing.
Severe solar elastosis.
Excessive subcutaneous fat in the area(s) to be treated.
Excessive skin laxity on the area(s) to be treated.
Significant scarring in the area(s) to be treated that would interfere with assessing results.
Open wounds or lesions in the area(s) to be treated.
Inability to understand the protocol or to give informed consent.
Microdermabrasion, or prescription level glycolic acid treatment to the treatment area(s) within four weeks prior to study participation or during the study.
Excessive dermatochalasis, deep dermal scarring, or thick sebaceous skin in the area(s) to be treated.
BMI equal to or greater than 30.
History of chronic drug or alcohol abuse.
History of collagen vascular disease.
History of autoimmune disease.
Subjects with implanted pacemaker or defibrillator.
Subjects with sensitivity or allergy to gold.
Subjects with sensitivity or allergy to pre-treatment medication.
Subjects with photosensitive skin.
Concurrent therapy that, in the investigator's opinion, would interfere with the evaluation of the safety or efficacy of the study device.
Subjects who anticipate the need for inpatient surgery or overnight hospitalization during the study.
Subjects who, in the investigator's opinion, have a history of poor cooperation, noncompliance with medical treatment, or unreliability.
Concurrent enrollment in any study involving the use of investigational devices or drugs.
Current smoker or history of smoking in the last five years.
Current user of any nicotine-containing products, e.g., e-cigarettes, Nicorette gum, nicotine patches, etc.
History of surgical or cosmetic treatments in the area(s) to be treated within the past year.
History or current use of the following prescription medications:
1. Accutane or other systemic retinoids within the past twelve months;
2. Topical Retinoids within the past two weeks; and/or
3. Antiplatelet agents/Anticoagulants (Coumadin, Heparin, Plavix) within the past two weeks.
Psychiatric drugs that in the investigators opinion would impair the subject from understanding the protocol requirements or understanding and signing the informed consent.