Mode
Text Size
Log in / Sign up
N/A N=25 Single-blind Treatment

Clinical Evaluation of Fractional Radiofrequency for the Treatment of Acne Scarring

Acne Scars

Enrolled (actual)
25
Serious AEs
0.0%
Results posted
Mar 2021
Primary outcome: Primary: Overall Acne Scar Improvement Assessed by the Global Aesthetic Improvement Scale (GAIS) at 12 Weeks. — 1.06; 0.85 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Venus Viva (Device)
Age
Adult, Older Adult · 22+ yrs
Sex
All
Sponsor
Venus Concept
Primary completion
Nov 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Acne Scar Improvement Assessed by the Global Aesthetic Improvement Scale (GAIS) at 12 Weeks.
1.06; 0.85
SECONDARY
Subject Satisfaction
3.25; 3.55; 3.18; 3.36
SECONDARY
Subject Scale - Visual Analog Scale for Pain
2.23; 2.05
SECONDARY
Number of Participants With Treatment-Related Adverse Events [Safety]
0; 0
SECONDARY
Subject Scale - 5 Point Scale for Treatment Tolerability
3.36; 3.48

Summary

Prospective, single centre, evaluator-blind study of the safety and performance of fractional radiofrequency (RF) for the treatment and reduction of acne scarring. The study will evaluate 50 treatment sites in subjects requesting treatment of their acne scarring. The study will involve three treatments on both sides of the face with 3-5 week intervals between each treatment. Subjects will be followed at 6 and 12 weeks after their last treatment. Analysis will be performed on all subjects who receive at least one treatment.

Eligibility Criteria

Inclusion Criteria

  • Healthy, male or female subjects 22 years of age or over who are seeking treatment and reduction of their facial acne scarring.
  • Able to read, understand and voluntarily provide written Informed Consent.
  • Able and willing to comply with the treatment/follow-up schedule and requirements.
  • 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

  • Implantable defibrillators, cardiac pacemakers, and other metal implants
  • Subjects with any implantable metal device in the treatment area
  • Pacemaker or internal defibrillator, or any other active electrical implant anywhere in the body (e.g. cochlear implant).
  • Permanent implant in the treated area, such as metal plates and screws, or an injected chemical substance.
  • Current or history of any kind of cancer, or pre-malignant moles.
  • Severe concurrent conditions, such as cardiac disorders.
  • Pregnancy or intending to become pregnant during the study and nursing.
  • Impaired immune system due to immunosuppressive diseases, such as AIDS and HIV, or use of immunosuppressive medications.
  • History of diseases stimulated by heat, such as recurrent herpes simplex in the treatment area; may be enrolled only after a prophylactic regime has been followed for 2 weeks or longer prior to enrollment, or according to Investigator's discretion .
  • Poorly controlled endocrine disorders, such as diabetes.
  • Any active condition in the treatment area, such as sores, psoriasis, eczema, and rash.
  • History of skin disorders, such as keloids, abnormal wound healing, as well as very dry and fragile skin.
  • History of bleeding coagulopathies, or use of anticoagulants (excluding daily aspirin).
  • Facial dermabrasion, facial resurfacing, or deep chemical peeling within the last three months, if face is treated.
  • Use of isotretinoin (Accutane®) or other retinoids within six months prior to treatment or as per physician's discretion.
  • Use of non-steroidal anti-inflammatory drugs (NSAIDS, e.g. ibuprofen-containing agents) one week before and after each treatment session.
  • Any surgical procedure in the treatment area within the last six months or before complete healing.
  • Treating over tattoo or permanent makeup.
  • Excessively tanned skin from sun, tanning beds or tanning creams within the last two weeks.
  • As per the practitioner's discretion, refrain from treating any condition which might make it unsafe for the patient.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03767153). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search