# Noninferiority Study Comparing the Efficacy and Safety of a New Hyaluronic Acid (HA) Filler Containing Lidocaine With an Existing HA Filler for the Treatment of Nasolabial Fold Wrinkles: A Randomized, Double‐Blind, Split‐Face Trial

## TL;DR

A new hyaluronic acid filler with lidocaine was found to be as effective and safe as an existing filler for treating nasolabial fold wrinkles over 48 weeks.

## Contribution

Demonstrated non-inferiority of a new HA filler with lidocaine compared to an existing HA filler in a 48-week clinical trial.

## Key findings

- WSRS scores at 24 and 48 weeks showed no significant difference between the new and existing fillers.
- GAIS scores at all follow-ups showed no significant differences between the two groups.
- Pain and swelling were common but not statistically significant compared to the control group.

## Abstract

The aesthetic use of hyaluronic acid (HA) has led to the development of various commercial HA fillers. Crosslinked HA dermal fillers are commonly used to treat facial wrinkles. This study demonstrated the non‐inferiority of the newly developed hyaluronic acid filler by comparing its efficacy and safety to that of the existing hyaluronic acid filler.

This 48‐week study was designed as a randomized, double‐blind, split‐face trial. Subjects who met the inclusion and exclusion criteria had a total of four follow‐up visits after receiving a dermal filler in the nasolabial folds. Efficacy was assessed using the Wrinkle Severity Rating Score (WSRS) and the Global Aesthetic Improvement Scale (GAIS). Safety was determined through the evaluation of laboratory tests, monitoring adverse events, and verifying vital signs.

WSRS measured at week 24 of the follow‐up visit showed no statistically significant difference, with scores of 2.02 ± 0.71 in the new filler group and 2.27 ± 0.68 in the existing filler group. Even at the 48‐week follow‐up visit, the improvement rate in the Wrinkle Severity Rating Scale (WSRS) of more than 1 point did not show a statistically significant difference between the new filler group and the existing filler group. The GAIS scores at each follow‐up visit showed no statistically significant differences between the two groups. The most frequently reported symptoms related to the test device during the 48‐week trial were pain and swelling. However, these symptoms were not statistically significant when compared to the control group from a treatment perspective.

In a 48‐week clinical trial aimed at treating nasolabial fold (NLF) wrinkles, the new hyaluronic acid (HA) filler demonstrated efficacy and safety comparable to that of existing control filler. As a result, the new HA filler is both an effective and safe option for improving NLF wrinkles.

This study was registered with ClinicalTrials.gov under the registration number NCT06310863