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Evaluation of Collagen Dermal Filler with Lidocaine for the Correction of Nasolabial Folds: A Randomized, Double-Blind, Multicenter Clinical Trial.

Authors :
Yang, Chin-Yi
Chang, Ya-Ching
Tai, Hao-Chih
Liao, Yi-Hua
Huang, Yu-Huei
Hui, Rosaline Chung-Yee
Kuo, Yuan-Sung
Horng, Shyue-Yih
Sheen, Yi-Shuan
Chen, Tim-Mo
Tzeng, Yuan-Sheng
Wang, Chih-Hsin
Teng, Shou-Cheng
Chang, Chun-Kai Oscar
Chou, Chang-Yi
Source :
Clinical, Cosmetic & Investigational Dermatology; Jul2024, Vol. 17, p1621-1631, 11p
Publication Year :
2024

Abstract

Purpose: Porcine-based dermal injectable collagen is effective for nasolabial fold correction. In the present study, a new dermal injectable collagen, incorporating a novel cross-linking technology and premixed with lidocaine, was introduced. The study aimed to determine the efficacy of the new dermal injectable collagen in improving bilateral nasolabial fold wrinkles, and reducing pain during injection. Patients and Methods: This prospective, double-blind, multicenter, parallel-group, randomized trial enrolled participants with moderate-to-severe bilateral nasolabial fold wrinkles from February 2019 to March 2021. Participants were randomly assigned to the test group (new dermal injectable collagen with lidocaine featuring a novel cross-linking technology) or control group (traditionally cross-linked dermal injectable collagen with lidocaine). Participants were monitored for adverse events (AEs), and for pain using the Thermometer Pain Scale (TPS) and a visual analog scale (VAS). Efficacy was measured using the Wrinkle Severity Rating Scale (WSRS) and the Global Aesthetic Improvement Scale (GAIS). Results: On the poor or better sides, the 2 groups exhibited a significant decrease in WSRS scores at 4, 12, 24, and 36 weeks after treatment, compared to baseline WSRS scores (all, p < 0.05). Compared to the control group, the test group had a greater decrease in WSRS score (poor or better sides) at 12, 24, 36, and 52 weeks after treatment (all, p < 0.05). A similar observation was also found in the WSRS response rate and GAIS score of the 2 groups. VAS and TPS scores were not significantly different between the 2 groups (p > 0.05), indicating that pain reduction was similar in the 2 groups. All AEs were anticipated AEs associated with facial aesthetic injections, and most recovered within 0 to 30 days without sequelae. There were no differences in AEs between the 2 groups (all, p > 0.05). Conclusion: The new dermal injectable collagen with lidocaine exhibited better efficacy for correcting nasolabial fold wrinkles compared to the control group. Both relieved pain and produced only transient and tolerable AEs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
11787015
Volume :
17
Database :
Complementary Index
Journal :
Clinical, Cosmetic & Investigational Dermatology
Publication Type :
Academic Journal
Accession number :
179051178
Full Text :
https://doi.org/10.2147/CCID.S447760