Fractional Radiofrequency for Reduction of Surgical Scar Formation
Study Details
Study Description
Brief Summary
Safety and Efficacy of Fractional Radiofrequency for the Reduction of Surgical Scar Formation
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
The study will evaluate up to 20 subjects scheduled to undergo breast reduction or breast mastectomy in which scar assessment can be made after pre-surgical treatment in a split-body design. The study will involve a single treatment of radiofrequency (RF) applied to one side of the surgical area(s) within 24 hours prior to the procedure. The subject will act as their own control, where one surgical area will be treated, and the other will not be and will act as the control. Tissue samples will be biopsied from the RF treated skin, as well as non-treated skin, at follow up visits. The samples will be used for histological evaluation to assess tissue structure and regeneration following surgery.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Treatment Group All enrolled subjects will undergo breast reduction or breast mastectomy in which scar assessment will be made after pre-surgical treatment in a split-body design, involving a single treatment of RF application to one side of the surgical area(s) within 24 hours prior to the procedure. The subject will act as their own control, where one surgical area will be treated, and the other will not be and will act as the control. Tissue samples will be biopsied from RF treated skin, as well as non-treated skin, at follow up visits. The samples will be used for histological evaluation to assess tissue structure and regeneration following surgery. |
Device: Fractional Radiofrequency
Fractional Radiofrequency (RF) delivering nano-fractional RF energy, causing fractional ablation and coagulation at the treatment site.
|
Outcome Measures
Primary Outcome Measures
- Independent blinded assessment [6-months after treatment]
Independent blinded evaluator assessment of the surgical scar sites using the Global Aesthetic Improvement Scale (GAIS), comparing follow-up visit photographs for both the treated and untreated sides.
- Principle Investigator (PI) evaluation of the scar(s) [3- and 6-months after treatment]
PI evaluation of the scar(s) using the Manchester Scar Scale (MSS) at 3 and 6 months post-treatment for both the treated and untreated sides. Non-invasive skin assessments will be evaluated to document scar morphology, scar thickness/density and colorimetry for both the treated and untreated sides.
Secondary Outcome Measures
- Subject Satisfaction [3- and 6-months after treatment]
Subject satisfaction of treatment using the Subject Satisfaction Scale
- Histological Assessment [1-, 3- and 6-months after treatment]
Histological assessment of the treated and the untreated (control) area.
- Scar Morphology [Baseline, 3- and 6-months after treatment]
Scar morphology will be digitally analyzed using 3D photography camera
- Ultrasonography [Baseline, 3- and 6-months after treatment]
High ultrasonography will be used to analyze scar thickness, epidermal thickness and skin density
- Colorimetry [Baseline, 3- and 6-months after treatment]
o Colorimetry assessment will be used to establish a clinically acceptable objective assessment of patients' scars
Eligibility Criteria
Criteria
Inclusion Criteria:
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Healthy, female subjects 21-75 years of age who are seeking pre-treatment for the prevention of surgical scars.
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Able to read, understand and voluntarily provide written Informed Consent.
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Able and willing to comply with the treatment/follow-up schedule and requirements.
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Willing to avoid direct sunlight to the treatment area for the duration of the study.
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Women of child-bearing age are required to be using a reliable method of birth control at least 3 months prior to study enrollment and for the duration of the study, and have a negative Urine Pregnancy test at baseline.
Exclusion Criteria:
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Subjects with any implantable metal device in the treatment area
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Pacemaker or internal defibrillator, or any other active electrical implant anywhere in the body (e.g. cochlear implant).
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Permanent implant in the treated area, such as metal plates and screws, or an injected chemical substance.
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Current or history of any kind of cancer, or dysplastic nevi.
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Severe concurrent conditions, such as cardiac disorders.
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Pregnancy or intending to become pregnant during the study and nursing.
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Impaired immune system due to immunosuppressive diseases, such as AIDS and HIV, or use of immunosuppressive medications.
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History of diseases stimulated by heat, such as recurrent herpes simplex in the treatment area; may be enrolled only following a prophylactic regime.
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Poorly controlled endocrine disorders, such as diabetes.
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Any active condition in the treatment area, such as sores, psoriasis, eczema, and rash.
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History of skin disorders, such as keloids, abnormal wound healing, as well as very dry and fragile skin.
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History of bleeding coagulopathies, or use of anticoagulants.
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Use of isotretinoin (Accutane®) within six months prior to treatment or at physician discretion.
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Treating over tattoo or permanent makeup.
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Excessively tanned skin from sun, tanning beds or tanning creams within the last two weeks.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | UT Southwestern Medical Center, Department of Plastic Surgery | Dallas | Texas | United States | 75390 |
Sponsors and Collaborators
- Venus Concept
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- VI0120