Treatment With the Evoke System for Facial and Submental Laxity

InMode

Status

Completed

Conditions

Laxity; Skin

Treatments

Device: Evoke radiofrequency device

Study type

Interventional

Funder types

Industry

Identifiers

NCT04719013

DO609886A

Details and patient eligibility

About

The aim of the study is to evaluate the efficacy, patient comfort, and patient satisfaction after Evoke treatment for face and submental area

Full description

The aim of the study is to evaluate the efficacy, patient comfort, and patient satisfaction after Evoke treatment for face and submental area Prospective, open label clinical study.

Enrollment

85 patients

Sex

All

Ages

35 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

- Signed informed consent to participate in the study.
Female and male subjects, 35 and 75 years of age at the time of enrolment
If female, not pregnant, lactating and must be either post-menopausal, surgically sterilized, or using a medically acceptable form of birth control at least 3 months prior to enrolment (i.e., oral contraceptives, contraceptive implant, barrier methods with spermicide or abstinence).
In addition, negative urine pregnancy test as tested before each treatment and at the last visit for women with childbearing potential (e.g. not menopause).
General good health confirmed by medical history and skin examination of the treated area.
Willing to have photographs and images taken of the treated areas to be used de-identified in evaluations, publications and presentations.
The patients should be willing to comply with the study procedure and schedule, including the follow up visit, and will refrain from using any other aesthetic treatment methods for the last 6 months and during the entire study period.

Exclusion criteria

- Pacemaker or internal defibrillator, or any other active electrical implant anywhere in the body.
Permanent implant in the treated area such as metal plates and screws, silicone implants or an injected chemical substance, unless deep enough in the periostal plane.
Current or history of skin cancer, or current condition of any other type of cancer, or premalignant moles.
Severe concurrent conditions, such as cardiac disorders, epilepsy, uncontrolled hypertension, and liver or kidney diseases.
Pregnancy and nursing.
Impaired immune system due to immunosuppressive diseases such as AIDS and HIV, or use of immunosuppressive medications.
Patients with history of diseases stimulated by heat, such as recurrent Herpes Simplex in the treatment area, may be treated only following a prophylactic regimen.
Poorly controlled endocrine disorders, such as diabetes or thyroid dysfunction.
Any active condition in the treatment area, such as sores, psoriasis, eczema, and rash.
History of skin disorders, keloids, abnormal wound healing, as well as very dry and fragile skin.
History of bleeding coagulopathies or use of anticoagulants in the last 10 days.
Any surgery in treated area within 3 months prior to treatment.
Six months delay is required if other recent treatments like light, CO2 laser or RF were performed on the same area.
Use of Isotretinoin (Accutane®) within 6 months prior to treatment.
Simultaneously participating in another investigator drug or device study or has completed the follow-up phase for the primary endpoint of any previous study less than 1 year prior to the first evaluation in this study.
As per the practitioner's discretion, refrain from treating any condition that might make it unsafe for the patient