Safety and Efficacy of the BTL-754 Device for Laser Skin Resurfacing Treatment of the Face

BTL

Status

Completed

Conditions

Wrinkle

Treatments

Device: BTL-754-4 Treatment

Study type

Interventional

Funder types

Industry

Identifiers

NCT06158438

BTL-754_CTBG100

Details and patient eligibility

About

This study will evaluate the clinical safety and the performance of the BTL-754 device (equipped with the 754-4 applicator) for reduction of facial wrinkles by the means of laser skin resurfacing treatment.

Enrollment

56 patients

Sex

All

Ages

22+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Healthy male or female subjects over 22 years of age seeking treatment for reduction of wrinkles.
Presence of clearly visible wrinkles in the treated area when the face is relaxed as deemed appropriate by the Investigator.
Subjects are willing to have polycarbonate eye shields placed for study treatment.
Subjects should be able to understand the investigative nature of the treatment, the possible benefits and side effects, and must sign the Informed Consent Form.
Subjects are willing to maintain the usual skin care regimen during study participation with the exception when protocol specified ointments, moisturizers, and cleansers are required during the healing stage. Sunblock is required throughout the subject's participation in the study.
Subjects are willing to abstain from other facial cosmetic procedures during the study; examples include, but are not limited to: laser or chemical resurfacing, dermabrasion, neuromodulator and/or filler injections, aesthetic facial surgery, etc.
Subjects are willing and able to comply with protocol requirements, including obtaining study-required digital photographs and assessments, post-care instructions, and returning for follow-up visits.
Women of childbearing potential are required to use birth control measures.

Exclusion criteria

Intolerance to anesthetic based agents
Infectious disease
Connective tissue disease
Propensity for keloid formations
Immunocompromised or compromised healing
Use of long-standing systemic steroids (e.g. Prednisone, Dexamethasone)
Pregnant, planning to become pregnant, or breast feeding during the study
Use of isotretinoin (e.g. Accutane, Sotret, Claravis, Amnesteem) within the past year
Medical condition that may affect wound healing
Any unstable medical or psychiatric conditions
Major systemic diseases - e.g. uncontrolled Diabetes mellitus
Photosensitivity, medications affecting sensitivity to light
Corticosteroids or injections of the treated area within the last 90 days, long-term corticosteroids use
Electronic implants (such as cardiac pacemakers, defibrillators and neurostimulators)
Blepharoplasty (in case of eyelid treatment)
Anticoagulant therapy, bleeding disorders
Application within 4 to 6 months after radiotherapy
Known or suspected malignancy, history of cancer or any type of malignancy
Febrile conditions, serious illness, chronic infection
Epilepsy
Deep vein thrombosis
Subject has had concurrent therapy that, in the investigator's opinion, would interfere with the evaluation of the safety and effectiveness of the study treatment method.
Subject is enrolled in another investigational (drug or device) clinical trial or has participated in any other investigational study within 30 days prior to consent that can interfere with this study's assessments as per investigator's discretion.
Subject has undergone a facelift procedure, IPL, laser, microneedling, chemical peels, dermal fillers, BOTOX® or other toxins within 6 months prior to the screening visit.
Tattoo(s) or permanent make-up in the intended treatment area.
Subject has used, within 30 days prior to screening or plans to use during study participation, Accutane, Retinol, or any medication that can cause dermal hypersensitivity.
Any other disease or condition at the investigator discretion that may pose risk to the patient or compromise the study.