Suppr超能文献

贝美前列素 0.01%治疗眉毛稀疏症的疗效和安全性:一项随机、双盲、对照研究。

Efficacy and Safety of Bimatoprost 0.01% for the Treatment of Eyebrow Hypotrichosis: A Randomized, Double-Blind, Vehicle-Controlled Study.

机构信息

*All authors are affiliated with the Division of Dermatology, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

All authors are affiliated with the Division of Dermatology, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

出版信息

Dermatol Surg. 2019 Dec;45(12):1549-1556. doi: 10.1097/DSS.0000000000001944.

Abstract

BACKGROUND

Eyebrow hypotrichosis is an important dermatological problem. However, there is no standard treatment.

OBJECTIVE

To study the efficacy and safety of bimatoprost 0.01% for the treatment of eyebrow hypotrichosis.

MATERIALS AND METHODS

Although bimatoprost 0.03% has been studied previously, this is the first study to evaluate the efficacy and safety of bimatoprost 0.01% for the treatment of eyebrow hypotrichosis. A randomized, double-blinded, vehicle-controlled trial was conducted in 40 patients. All patients were randomized to receive bimatoprost 0.01% or placebo vehicle, once daily, for 6 months. The primary outcome was improvement in eyebrow density and diameter. Additional outcomes were the improvement in clinical assessments and safety evaluation.

RESULTS

Compared to the vehicle group, bimatoprost 0.01% significantly increased mean eyebrow hair density, eyebrow hair diameter, and clinical assessments (p < .001) in the drug group. Patients' satisfaction score was higher for the drug group than the vehicle group (p < .05). Adverse effects of the treatment were minimal and similar between the 2 groups.

CONCLUSION

Bimatoprost 0.01% was found to be superior to a placebo for eyebrow enhancement. Bimatoprost 0.01% can be considered effective, safe, and well-tolerated for the treatment of eyebrow hypotrichosis.

摘要

背景

眉毛稀疏是一个重要的皮肤学问题,但目前尚无标准的治疗方法。

目的

研究 0.01%比马前列素治疗眉毛稀疏的疗效和安全性。

材料和方法

虽然之前已经研究过 0.03%的比马前列素,但这是首次评估 0.01%比马前列素治疗眉毛稀疏的疗效和安全性的研究。对 40 例患者进行了一项随机、双盲、对照试验。所有患者均随机接受 0.01%比马前列素或安慰剂,每日 1 次,治疗 6 个月。主要终点为眉毛密度和直径的改善。次要终点为临床评估和安全性评估的改善。

结果

与安慰剂组相比,0.01%比马前列素组的眉毛毛发密度、直径和临床评估均显著增加(p<0.001)。药物组患者的满意度评分高于安慰剂组(p<0.05)。两组的不良反应均较少且相似。

结论

0.01%比马前列素在眉毛增浓方面优于安慰剂。0.01%比马前列素治疗眉毛稀疏有效、安全且耐受良好。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验