首页> 外文期刊>Clinical, Cosmetic and Investigational Dermatology >Clinical evidence on the efficacy and tolerability of a topical medical device containing benzoylperoxide 4%, retinol 0.5%, mandelic acid 1% and lactobionic acid 1% in the treatment of mild facial acne: an open label pilot study
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Clinical evidence on the efficacy and tolerability of a topical medical device containing benzoylperoxide 4%, retinol 0.5%, mandelic acid 1% and lactobionic acid 1% in the treatment of mild facial acne: an open label pilot study

机译:含有4%苯甲酰过氧化物,0.5%视黄醇,1%扁桃酸和1%乳糖酸的局部医疗器械在治疗轻度面部痤疮中的功效和耐受性的临床证据:一项开放性试验研究

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Background: Acne is a debilitating disorder that requires proper treatment depending on the clinical manifestations and pathogenetic factors, among which hyper-keratinization, seborrhea and bacterial proliferation. Combining active ingredients targeting the different mediators of acne pathogenesis may yield optimal outcomes. Purpose: The purpose of this study was to evaluate the clinical effectiveness, safety and tolerability of a new topical medical device in cream containing benzoylperoxide 4%, pure retinol 0.05%, palmitate retinol 0.5%, mandelic acid 1% and glycyrrhetic acid on patients with mild acne. Patients and methods: Twenty consecutive patients of both sexes with mild acne were included in the study. The topical treatment was self-applied twice a day for 12?weeks. Evaluations included: Global Acne Grading System (GAGS); inflammatory and non-inflammatory lesions count; reflectance confocal microscopy; seborrhea and hydration degree; photographic documentation; a questionnaire to assess tolerability. Results: The GAGS score showed a 39% reduction from T0 to T1 and 69.20% from T0 to T2. The count of comedonic lesions showed a 44% reduction from T0 to T1 and 65% from T0 to T2. The count of papular lesions diminished by 49.4% from T0 to T1 and by 62% from T0 to T2. The count of pustular lesions decreased by 43% from T0 to T1 and by 80% from T0 to T2. Improvement of hydration and a decrease of seborrhea degree were even observed. These clinical results were confirmed by reflectance confocal microscopy exam. Conclusion: The topical medical device has shown to be clinically effective and well tolerated for the treatment of mild acne. Side effects were mild, transient and well tolerated. The results of our study demonstrated a high tolerability of this new combination of benzoylperoxide 4% and retinol. Furthermore, our results suggested that the studied compound could be considered as a “maintenance treatment” after specific pharmacological treatment, even in more severe types of acne.
机译:背景:痤疮是一种使人衰弱的疾病,需要根据临床表现和致病因素(包括过度角化,皮脂溢和细菌增殖)进行适当的治疗。结合针对痤疮发病机制的不同介质的活性成分可能会产生最佳结果。目的:本研究的目的是评估一种新型局部医疗器械在含过氧化苯甲酰过氧化物4%,纯视黄醇0.05%,棕榈酸酯视黄醇0.5%,扁桃酸1%和甘草酸的乳膏中的临床有效性,安全性和耐受性。轻度痤疮。患者和方法:本研究包括连续20名男女中度痤疮。每天两次局部应用局部治疗,持续12周。评估包括:全球痤疮分级系统(GAGS);炎性和非炎性病变计数;反射共聚焦显微镜皮脂溢出和水合作用程度;摄影文件;评估耐受性的问卷。结果:GAGS评分显示从T0到T1降低39%,从T0到T2降低69.20%。粉刺病变的数量显示从T0到T1减少了44%,从T0到T2减少了65%。从T0到T1,丘疹病变的数量减少了49.4%,从T0到T2减少了62%。脓疱病变的数量从T0到T1减少了43%,从T0到T2减少了80%。甚至观察到水合作用改善和皮脂溢出程度降低。这些临床结果通过反射共聚焦显微镜检查得到证实。结论:局部医疗器械已显示出对轻度痤疮的临床疗效和良好的耐受性。副作用轻微,短暂且耐受良好。我们的研究结果表明,这种4%的过氧化苯甲酰和视黄醇的新组合具有很高的耐受性。此外,我们的结果表明,即使在更严重的痤疮类型中,也可以将经过研究的化合物视为经过特殊药物治疗后的“维持治疗”。

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