Clinical Evaluation of a Cross-Linked Hyaluronic Acid Dermal Filler Applied for Facial Augmentation

January 2015 | Volume 14 | Issue 1 | Original Article | 19 | Copyright © January 2015


Scott KM Barr MD FRCPC,a Arie Benchetrit MD FRCPC,b Mariusz Sapijaszko MD FRCP,c
and Anneke Andriessen PhDd

aBarr Plastic Surgery, Consultant Skin MediSpa, Sudbury, Ontario, Canada
bCosmedica Clinic, Pointe-Claire, Québec, Canada
cYouthful Image Clinic, Medical Director, Edmonton, Alberta, Canada
dAndriessen Consultants, Nijmegen, The Netherlands

Abstract
BACKGROUND: Hyaluronic Acid (HA) fillers are widely used for restoring facial volume.
OBJECTIVE: A 24-week study evaluated clinical efficacy with HA.
METHODS AND MATERIALS: Included were 15 healthy subjects recruited from 4 centers, between ages of 35 to 65 years, who had a Wrinkle Severity Rating Scale (WSRS) score ≥ 3, indicating moderate volume loss. Revanesse® Ultra (Prollenium), a HA dermal filler, was used. Primary study outcome was physicians scored facial volume correction, using the Global Aesthetic Improvement Scale (GAIS), comparing baseline (day 0) versus 24 weeks (end) and blindly assessed photographs. Subject satisfaction and comfort was evaluated using self-administered questionnaires at day 0 and at week 24.
RESULTS: N = 15, 13 female and 2 males with a mean age (years) of 48.52 ( SD ± 10.46) received treatment with HA and completed the 24-week study. At screening they had a moderate (mean 2.85, SD ± 0.45) WSRS score. At week 24 a market facial volume restoration was shown and no adverse events were reported. All patients reported to be satisfied with the obtained results.
CONCLUSION: Good – excellent volume enhancement was noted almost immediately after the HA injections, improving patient reported quality of life aspects. HA treatment was shown to be safe.

J Drugs Dermatol. 2015;14(1):19-23.

INTRODUCTION

MATERIALS AND METHODS

Study Objectives

Primary objective: Physician assessed clinical efficacy
  • Restoring facial volume resulting in a correction of nasolabial folds, mesolabial folds and vermillion border lines, using the GAIS [10,11] comparing baseline (day 0) versus 24 weeks (end).
  • Blindly assessed standardized photographs at baseline and at 24 weeks (end).
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