A randomized interventional study that compares treatments for vitiligo and anti-vitiligo cream.

IF 1.8 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Shahzad Shirzad, Mahdis Miladi
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引用次数: 0

Abstract

This study aimed to evaluate the efficacy of a novel combination therapy, AVC (Anti-Vitiligo Cream), compared to common treatments for vitiligo. A randomized interventional study was conducted on 1,000 patients with confirmed vitiligo, aged 7-70 years. Participants were divided into five groups (200 patients each): oral prednisolone, Tofacitinib, Ruxolitinib, AVC (Anti-Vitiligo Cream), and AVC combined with Tofacitinib. Outcomes were assessed over two years using the Vitiligo Area Scoring Index (VASI), patient satisfaction scores, and clinical observations. AVC-based therapies (Groups 4 and 5) demonstrated superior efficacy and patient satisfaction compared to other treatments. Group 5 (AVC + Tofacitinib) achieved the highest outcomes, with a mean satisfaction score of 90 (IQR: 85-95) and treatment efficacy significantly higher than Group 1 (p < 0.001). Regression analysis identified treatment outcomes and therapy type as significant predictors of satisfaction. AVC (Anti-Vitiligo Cream), particularly in combination with Tofacitinib, represents a groundbreaking approach for managing vitiligo, providing enhanced efficacy and patient satisfaction. These findings support the potential of AVC-based therapies as a standard treatment option.

一项比较白癜风和抗白癜风霜治疗的随机介入研究。
本研究旨在评估一种新型联合疗法AVC(抗白癜风霜)的疗效,与普通白癜风治疗方法相比。一项随机介入研究对1000例确诊白癜风患者进行了研究,年龄在7-70岁之间。参与者被分为五组(每组200例):口服强的松龙、托法替尼、鲁索利替尼、AVC(抗白癜风霜)和AVC联合托法替尼。通过白癜风区域评分指数(VASI)、患者满意度评分和临床观察来评估两年内的结果。与其他治疗相比,avc为基础的治疗(第4组和第5组)显示出更好的疗效和患者满意度。5组(AVC + Tofacitinib)疗效最高,平均满意度评分为90分(IQR: 85 ~ 95),治疗疗效显著高于1组(p < 0.001)。回归分析确定治疗结果和治疗类型是满意度的重要预测因子。AVC(抗白癜风霜),特别是与托法替尼的结合,代表了一种突破性的方法来管理白癜风,提供更高的疗效和患者满意度。这些发现支持以avc为基础的疗法作为标准治疗选择的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Journal of Translational Myology
European Journal of Translational Myology MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.30
自引率
27.30%
发文量
74
审稿时长
10 weeks
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