Feasibility Study To Collect Safety And Preliminary Efficacy Data For A Radiofrequency Microneedling Device

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 10

Inclusion Criteria

A healthy, non-smoking male or female between the age of 18-60 years old.
Fitzpatrick skin type I to VI.
Understands and accepts obligation not to receive any other procedures on the treatment area through the length of the study.
Understands and accepts the obligation and is logistically able to be present for all visits.
Is willing to comply with all requirements of the study and sign the informed consent document.

Exclusion Criteria

Is pregnant or of childbearing potential and not using medically effective birth control, or has been pregnant in the last 3 months, currently breast feeding or planning a pregnancy during the study.
The subject is currently enrolled in an investigational drug or device trial or has received an investigational drug or been treated with an investigational device within in the area to be treated 3 months prior to entering this study.
The subject has a pacemaker.
The subject had previous use of gold thread skin rejuvenation.
The subject has a cut, wound, or infected skin on the area to be treated (but skin eruptions may be treated).
The subject has a metal implant that interferes with the transmission of energy to the electrical field.
The subject has any embedded electronic devices that give or receive a signal.
The subject has Implantable Cardiac Defibrillators (ICD) or Cardiac Resynchronization Therapy (CRT) devices: treatment may interfere with the functionality of the device and/or damage the electronic implant.
The subject is allergic to adhesives such as glues on medical tape: they should be alerted that a rash may occur on the neutral electronic monitoring pad (NEM or neutral pad) site, and an over-the-counter preparation may be used to treat the area.
The subject is allergic to gold.
The subject has an unrealistic expectation of the results: this is not plastic surgery, and all subjects should be fully informed of the treatment's expected results.
The subject has nerve insensitivity to heat in the treatment area or in the neutral pad placement area.
The subject has severe laxity or sagging that causes redundant folds of tissue or hanging skin in the area to be treated: this treatment will be ineffective.
The subject has used Accutane (isotretinoin) six to twelve months prior to treatment, as this can thin the skin and make it brittle.
The subject is taking aspirin or are currently taking antiplatelets, thrombolytics, anti-inflammatories or anticoagulants.
The subject has a history of bleeding coagulopathies.
The subject is allergic to topical anesthetic.
The subject has any of the following conditions:
- Diabetes
- Epilepsy
- Autoimmune disease
- Herpes simplex
- HIV
- Hypertension
- Dermatitis
The subject has keloid formation propensity.
Subjects with electronic implants such as cardiac defibrillator. It may interfere with operation of electronic implants or damage the implants, causing risks.
The subject has any condition or is in a situation which in the investigators opinion may put the subject at significant risk, may confound study results or may interfere significantly with the subject's participation.

Cautionary Criteria:

The subject is prone to fever blisters: they should receive a prophylactic antiviral medication regimen prior to treatment.
The subject has lesions in the treatment area that have not been evaluated and diagnosed: they should be evaluated prior to the treatment day.
The subject has malignant disease (excluding skin malignancies).
The subject has used retinoids in the last seven days in the area to be treated: retinoids can create erythema and cause the skin to become heat sensitive.
The subject has used any chemical peels in the last two to three months in the treatment area: subjects should wait until any remaining erythema or side effects have resolved.
The subject has tattoos, permanent makeup, and permanent brows in the treatment area: caution must be used. (The ink used in these applications is unregulated and may have metallic components.)
The subject has a neuropathic disorder, impaired skin sensation or diabetic neuropathy.
The subject has received fillers or neurotoxin injections: subjects should wait two weeks before receiving a Potenza treatment.

Study & Design

Study Type: INTERVENTIONAL

Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Treatment with RF Device	RF Device (Potenza™)	Subjects may receive up to 3 treatments with the RF device if they are willing to receive treatment for brow lifting and/or present with conditions such as, but not limited to; wrinkles, fine lines, crepey skin, acne scars, active acne, enlarged pores, loose skin on the face, neck and/or body

Primary Outcome Measures

Name	Time	Method
Evaluation of Baseline Photographs Compared to Post Treatment Images	30 day follow up	Photographs will be evaluated at the baseline and the 30 day follow up. The number of photographs with improvement (based on changes in the skin) from baseline to follow up images will be reported.

Secondary Outcome Measures