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Safe and Effective Lip Enhancement with VYC-15L in Chinese Adults
BACKGROUND: Hyaluronic acid (HA) soft tissue fillers are used to restore volume loss to the lips and perioral area. OBJECTIVE: Evaluate the safety and effectiveness of the HA filler Juvéderm(®) Volbella(®) (VYC-15L) for lip enhancement in Chinese adults. METHODS & MATERIALS: In this multicenter,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661899/ https://www.ncbi.nlm.nih.gov/pubmed/36387967 http://dx.doi.org/10.2147/CCID.S382194 |
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author | Li, Dong Gao, Zhanwei Sun, Jiaming Li, Qin Jiang, Ping Zhang, Lijuan Chawla, Smita |
author_facet | Li, Dong Gao, Zhanwei Sun, Jiaming Li, Qin Jiang, Ping Zhang, Lijuan Chawla, Smita |
author_sort | Li, Dong |
collection | PubMed |
description | BACKGROUND: Hyaluronic acid (HA) soft tissue fillers are used to restore volume loss to the lips and perioral area. OBJECTIVE: Evaluate the safety and effectiveness of the HA filler Juvéderm(®) Volbella(®) (VYC-15L) for lip enhancement in Chinese adults. METHODS & MATERIALS: In this multicenter, evaluator-blind study, subjects seeking lip enhancement were randomized 3:1 to VYC-15L or no-treatment control group (with optional treatment delayed by 3 months). Effectiveness endpoints included 1-point improvement on the 5-point Lip Fullness Scale (LFS) assessed by evaluating investigators (EIs) and subjects, and overall volume of lips and change in lip surface area measured from 3-dimensional images. Safety assessments included procedural pain, injection site reactions (ISRs), and adverse events (AEs). RESULTS: The modified intention-to-treat population included 163 subjects (median age, 34 years; 96.9% female). More VYC-15L-treated subjects had a 1-point reduction in EI-reported LFS score at month 3 versus untreated controls (84.7% vs 0%; p < 0.0001), and 65% of the treated subjects self-reported a 1-point LFS improvement at month 3. Procedural pain during injection was mild. The most common ISRs were swelling, tenderness to touch, and firmness. One treatment-related serious AE (injection site compression arterial ischemia) resolved in 16 days. CONCLUSION: VYC-15L treatment was superior to no treatment at 3 months and was well tolerated by subjects. CLINICAL TRIAL REGISTRATION NUMBER: NCT03519204. |
format | Online Article Text |
id | pubmed-9661899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-96618992022-11-15 Safe and Effective Lip Enhancement with VYC-15L in Chinese Adults Li, Dong Gao, Zhanwei Sun, Jiaming Li, Qin Jiang, Ping Zhang, Lijuan Chawla, Smita Clin Cosmet Investig Dermatol Original Research BACKGROUND: Hyaluronic acid (HA) soft tissue fillers are used to restore volume loss to the lips and perioral area. OBJECTIVE: Evaluate the safety and effectiveness of the HA filler Juvéderm(®) Volbella(®) (VYC-15L) for lip enhancement in Chinese adults. METHODS & MATERIALS: In this multicenter, evaluator-blind study, subjects seeking lip enhancement were randomized 3:1 to VYC-15L or no-treatment control group (with optional treatment delayed by 3 months). Effectiveness endpoints included 1-point improvement on the 5-point Lip Fullness Scale (LFS) assessed by evaluating investigators (EIs) and subjects, and overall volume of lips and change in lip surface area measured from 3-dimensional images. Safety assessments included procedural pain, injection site reactions (ISRs), and adverse events (AEs). RESULTS: The modified intention-to-treat population included 163 subjects (median age, 34 years; 96.9% female). More VYC-15L-treated subjects had a 1-point reduction in EI-reported LFS score at month 3 versus untreated controls (84.7% vs 0%; p < 0.0001), and 65% of the treated subjects self-reported a 1-point LFS improvement at month 3. Procedural pain during injection was mild. The most common ISRs were swelling, tenderness to touch, and firmness. One treatment-related serious AE (injection site compression arterial ischemia) resolved in 16 days. CONCLUSION: VYC-15L treatment was superior to no treatment at 3 months and was well tolerated by subjects. CLINICAL TRIAL REGISTRATION NUMBER: NCT03519204. Dove 2022-11-10 /pmc/articles/PMC9661899/ /pubmed/36387967 http://dx.doi.org/10.2147/CCID.S382194 Text en © 2022 Li et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Li, Dong Gao, Zhanwei Sun, Jiaming Li, Qin Jiang, Ping Zhang, Lijuan Chawla, Smita Safe and Effective Lip Enhancement with VYC-15L in Chinese Adults |
title | Safe and Effective Lip Enhancement with VYC-15L in Chinese Adults |
title_full | Safe and Effective Lip Enhancement with VYC-15L in Chinese Adults |
title_fullStr | Safe and Effective Lip Enhancement with VYC-15L in Chinese Adults |
title_full_unstemmed | Safe and Effective Lip Enhancement with VYC-15L in Chinese Adults |
title_short | Safe and Effective Lip Enhancement with VYC-15L in Chinese Adults |
title_sort | safe and effective lip enhancement with vyc-15l in chinese adults |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661899/ https://www.ncbi.nlm.nih.gov/pubmed/36387967 http://dx.doi.org/10.2147/CCID.S382194 |
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