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含利多卡因的胶原蛋白真皮填充剂用于矫正鼻唇沟的评估:一项随机、双盲、多中心临床试验。

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

作者信息

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

机构信息

Department of Dermatology, New Taipei Municipal TuCheng Hospital, New Taipei City, 236, Taiwan.

Department of Dermatology, Linkou Chang-Gung Memorial Hospital, Taoyuan, 333, Taiwan.

出版信息

Clin Cosmet Investig Dermatol. 2024 Jul 8;17:1621-1631. doi: 10.2147/CCID.S447760. eCollection 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.

摘要

目的

猪源性可注射真皮胶原蛋白对改善鼻唇沟有效。在本研究中,引入了一种采用新型交联技术并预混利多卡因的新型可注射真皮胶原蛋白。本研究旨在确定这种新型可注射真皮胶原蛋白在改善双侧鼻唇沟皱纹及减轻注射过程中疼痛方面的疗效。

患者与方法

这项前瞻性、双盲、多中心、平行组、随机试验纳入了2019年2月至2021年3月有中度至重度双侧鼻唇沟皱纹的参与者。参与者被随机分配到试验组(采用新型交联技术且含利多卡因的新型可注射真皮胶原蛋白)或对照组(传统交联且含利多卡因的可注射真皮胶原蛋白)。对参与者进行不良事件(AE)监测,并使用温度计疼痛量表(TPS)和视觉模拟量表(VAS)评估疼痛情况。使用皱纹严重程度评分量表(WSRS)和整体美学改善量表(GAIS)评估疗效。

结果

在较差侧或较好侧,与治疗前基线WSRS评分相比,两组在治疗后4周、12周、24周和36周时WSRS评分均显著降低(均为p < 0.05)。与对照组相比,试验组在治疗后12周、24周、36周和52周时较差侧或较好侧的WSRS评分降低幅度更大(均为p < 0.05)。两组的WSRS有效率和GAIS评分也有类似结果。两组间VAS和TPS评分无显著差异(p > 0.05),表明两组疼痛减轻程度相似。所有不良事件均为与面部美容注射相关的预期不良事件,多数在0至30天内恢复,无后遗症。两组不良事件无差异(均为p > 0.05)。

结论

与对照组相比,含利多卡因的新型可注射真皮胶原蛋白在改善鼻唇沟皱纹方面疗效更佳。两者均能减轻疼痛,且仅产生短暂且可耐受的不良事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a5/11244637/c4b8bf959fcf/CCID-17-1621-g0001.jpg

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