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Study identifier: NCT07398768 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Prospective, Non-interventional Study Assessing Perioral Rejuvenation Procedure

Condition: Perioral Wrinkles · Crow's Feet · Lip Volume Enhancement  ·  Sponsor: Yuvell

PhaseN/A
Planned participants34
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

The goal of this observational study is to learn how a perioral rejuvenation procedure affects perioral line severity and lip volume over time in adults undergoing routine aesthetic treatment in a single clinical center. The main questions it aims to answer are: * What proportion of participants achieves a ≥1-point improvement from baseline on both the Lip Fullness Scale (LFS) and the Static Perioral Lines Assessment Scale (SPLAS) at Week 12? * How do skin wrinkling/surface roughness, lip and perioral volume, and patient satisfaction change over 6 and 12 weeks? Participants will: * Receive a routine (non-study-mandated) holistic perioral rejuvenation procedure as decided by their treating clinician. * Attend study visits at approximately baseline, Week 6, and Week 12. * Undergo independent clinical assessments (assessor not involved in treatment delivery) of LFS and SPLAS. * Have skin wrinkling and surface roughness documented by VISIA skin analysis (baseline, Week 6, Week 12). * Have lip and perioral volume measured by VECTRA M3 volume analysis (baseline, Week 6, Week 12). * Complete a standardized patient satisfaction questionnaire (Week 12).

This description comes directly from the study's public registry record.

Talk to the study team

Mia Cajkovsky  ·  +43 1 512 13 25 30  ·  mia.cajkovsky@yuvell.at

Michelle Friedrich, MSc  ·  +43 1 512 13 25 30  ·  michelle.friedrich@yuvell.at

Always discuss trial participation with your own doctor first.

Locations (1)

YUVELLVienna, State of Vienna, AustriaRecruiting

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Source record: clinicaltrials.gov/study/NCT07398768