Safe and Effective Chin Augmentation With the Hyaluronic Acid Injectable Filler, VYC-20L.
Abstract
[BACKGROUND] VYC-20L is a hyaluronic acid soft tissue filler with lidocaine designed to restore facial volume.
[OBJECTIVE] Evaluate the safety and effectiveness of VYC-20L in patients with chin retrusion.
[MATERIALS AND METHODS] Adults with chin retrusion were randomized (3:1) to receive VYC-20L in the chin at study onset (treatment group) or 6 months later (control group). The primary effectiveness end point was ≥1-point improvement on the Allergan Chin Retrusion Scale (ACRS) from baseline at Month 6. Safety assessments included injection site responses (ISRs) and adverse events (AEs).
[RESULTS] VYC-20L was administered to 192 participants (treatment group, n = 144; control group, n = 48). At Month 6, significantly more participants had an ACRS response in the treatment versus control group (56.3% vs 27.5%; p = .0019). Effectiveness was also demonstrated by the proportion of participants with improved/much improved Global Aesthetic Improvement Scale scores and responses on the FACE-Q Satisfaction with Chin questionnaire and FACE-Q Psychological Wellbeing module. Treatment benefit remained evident at Month 12. Most common ISRs were tenderness (81.1%) and firmness (75.1%). One participant (0.5%) discontinued the study due to 2 treatment-related serious AEs of facial cellulitis and injection site inflammation, both resolved without sequelae.
[CONCLUSION] VYC-20L significantly improved an ACRS response and was generally safe and well tolerated.
[OBJECTIVE] Evaluate the safety and effectiveness of VYC-20L in patients with chin retrusion.
[MATERIALS AND METHODS] Adults with chin retrusion were randomized (3:1) to receive VYC-20L in the chin at study onset (treatment group) or 6 months later (control group). The primary effectiveness end point was ≥1-point improvement on the Allergan Chin Retrusion Scale (ACRS) from baseline at Month 6. Safety assessments included injection site responses (ISRs) and adverse events (AEs).
[RESULTS] VYC-20L was administered to 192 participants (treatment group, n = 144; control group, n = 48). At Month 6, significantly more participants had an ACRS response in the treatment versus control group (56.3% vs 27.5%; p = .0019). Effectiveness was also demonstrated by the proportion of participants with improved/much improved Global Aesthetic Improvement Scale scores and responses on the FACE-Q Satisfaction with Chin questionnaire and FACE-Q Psychological Wellbeing module. Treatment benefit remained evident at Month 12. Most common ISRs were tenderness (81.1%) and firmness (75.1%). One participant (0.5%) discontinued the study due to 2 treatment-related serious AEs of facial cellulitis and injection site inflammation, both resolved without sequelae.
[CONCLUSION] VYC-20L significantly improved an ACRS response and was generally safe and well tolerated.
추출된 의학 개체 (NER)
| 유형 | 영어 표현 | 한국어 / 풀이 | UMLS CUI | 출처 | 등장 |
|---|---|---|---|---|---|
| 재료 | hyaluronic acid
|
히알루론산 | dict | 2 | |
| 시술 | chin augmentation
|
턱끝성형술 | dict | 1 | |
| 시술 | filler
|
필러 주입술 | dict | 1 | |
| 시술 | soft tissue filler
|
필러 주입술 | dict | 1 | |
| 해부 | Retrusion
|
scispacy | 1 | ||
| 합병증 | cellulitis
|
감염 | dict | 1 | |
| 합병증 | facial
|
scispacy | 1 | ||
| 합병증 | chin retrusion
|
scispacy | 1 | ||
| 약물 | lidocaine
|
리도카인 | dict | 1 | |
| 약물 | [BACKGROUND] VYC-20L
|
scispacy | 1 | ||
| 약물 | [OBJECTIVE]
|
scispacy | 1 | ||
| 약물 | [RESULTS] VYC-20L
|
scispacy | 1 | ||
| 약물 | [CONCLUSION] VYC-20L
|
scispacy | 1 | ||
| 질환 | ACRS
→ Allergan Chin Retrusion Scale
|
scispacy | 1 | ||
| 질환 | tenderness
|
C0234233
Sore to touch
|
scispacy | 1 | |
| 질환 | inflammation
|
C0021368
Inflammation
|
scispacy | 1 | |
| 질환 | AEs
→ adverse events
|
scispacy | 1 | ||
| 기타 | patients
|
scispacy | 1 | ||
| 기타 | participants
|
scispacy | 1 |
MeSH Terms
Adult; Aged; Aged, 80 and over; Cellulitis; Chin; Cosmetic Techniques; Dermal Fillers; Esthetics; Female; Gels; Humans; Hyaluronic Acid; Injection Site Reaction; Male; Middle Aged; United States
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