This study will collect effectiveness and safety data on JUVÉDERM VOLUX® Injectable Gel for Chin Enhancement in Chinese Adults based on real world data.
There will be 30 participants selected who undergo 3D imaging before and after JUVÉDERM VOLUX® treatment for digital analysis assessments. Up to 90 participants enrolled either prospectively prior to JUVÉDERM VOLUX® treatment or retrospectively after JUVÉDERM VOLUX® treatment.
Study Type
OBSERVATIONAL
Enrollment
90
JUVÉDERM VOLUX® injectable gel
Hainan Boao Super Hospital /ID# 235968
Qionghai, Hainan, China
Change from Baseline in the Glabella-Subnasale-Pogonion (G-Sn-Pog) Angle
Time frame: Baseline, Month 3
Percentage of Responders based on the Investigator's Assessment of Improvement in the Chin and Jaw Area using the 5-point Global Aesthetic Improvement Scale (GAIS)
The Evaluating Investigator will assess the aesthetic improvement of the hands using the GAIS 5- point scale where: 2=much improved, 1=improved, 0=no change, -1=worse and -2=much worse.
Time frame: Month 3
Percentage of Responders based on the Participant's Assessment of Improvement in the Chin and Jaw Area using the 5-point GAIS
Participant will assess the aesthetic improvement of the hands using the GAIS 5-point scale where: 2=much improved, 1=improved, 0=no change, -1=worse and -2=much worse.
Time frame: Month 3
The presence and severity of ISRs (Injection Site Response) at scheduled follow-up visits
The number of patients who experienced ISRs
Time frame: Month 1, 3, 6, and 12
The number of Adverse Events (AEs) from physician observation and inquiry at scheduled follow-up visits
The number of patients who experienced AEs
Time frame: Month 1, 3, 6, and 12
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