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一种非处方1%胶态燕麦片乳膏治疗儿童轻至中度特应性皮炎的疗效和安全性:一项双盲、随机、活性对照研究。

Efficacy and safety of an over-the-counter 1% colloidal oatmeal cream in the management of mild to moderate atopic dermatitis in children: a double-blind, randomized, active-controlled study.

作者信息

Lisante Toni Anne, Nuñez Chris, Zhang Paul

机构信息

a Research & Development Clinical Research , Johnson & Johnson Consumer Inc , Skillman , NJ , USA.

b Research & Development Biostatistics , Johnson & Johnson Consumer Inc , Skillman , NJ , USA.

出版信息

J Dermatolog Treat. 2017 Nov;28(7):659-667. doi: 10.1080/09546634.2017.1303569. Epub 2017 Apr 2.

Abstract

PURPOSE

The purpose of this study is to evaluate the efficacy and safety of an over-the-counter (OTC) 1% colloidal oatmeal cream versus a prescription barrier cream in children with mild-to-moderate atopic dermatitis (AD).

MATERIALS AND METHODS

Eligible patients (6 months-18 years) were randomized to OTC or prescription cream. Eczema Area and Severity Index (EASI) scores, Investigator's Global Atopic Dermatitis Assessment (IGADA) scores, patients' and/or caregivers' assessment of itch using 10-cm visual analog scale (VAS) on day 0, weeks 1, 2, and 3 were assessed. The intention to treat (ITT) and per protocol (PP) populations were analyzed.

RESULTS

Ninety patients (mean [SD] age, 8.1 [4] years; boys, 45.6%; African American, 54.4%) were randomized (OTC cream, 45; prescription cream, 45). At week 3, EASI scores showed that the OTC cream was non-inferior (non-inferiority margin = 1.5) to the prescription cream (adjusted mean change [95% CI] from baseline: ITT, 0.18 [-0.35, 0.70]; PP, 0.14 [-0.42, 0.70]). IGADA (adjusted mean between group difference, 0.106 [-0.130, 0.341]) and VAS itch (0.103 [-0.831, 1.038]) scores improved in both groups. No safety issues were identified.

CONCLUSION

OTC 1% oatmeal cream was equally effective and safe as the prescription barrier cream for the symptomatic treatment of mild-to-moderate AD in children.

TRIAL REGISTRATION NUMBER

NCT01326910.

摘要

目的

本研究旨在评估非处方(OTC)1%胶态燕麦片乳膏与处方屏障乳膏治疗轻至中度特应性皮炎(AD)患儿的疗效和安全性。

材料与方法

符合条件的患者(6个月至18岁)被随机分配至使用OTC乳膏或处方乳膏组。在第0天、第1、2和3周评估湿疹面积和严重程度指数(EASI)评分、研究者整体特应性皮炎评估(IGADA)评分、患者和/或护理人员使用10厘米视觉模拟量表(VAS)对瘙痒的评估。对意向性治疗(ITT)人群和符合方案(PP)人群进行分析。

结果

90例患者(平均[标准差]年龄,8.1[4]岁;男孩,45.6%;非裔美国人,54.4%)被随机分组(OTC乳膏组45例;处方乳膏组45例)。在第3周时,EASI评分显示OTC乳膏不劣于(非劣效界值 = 1.5)处方乳膏(从基线调整后的平均变化[95%CI]:ITT,0.18[-0.35, 0.70];PP,0.14[-0.42, 0.70])。两组的IGADA(组间调整后的平均差异,0.106[-0.130, 0.341])和VAS瘙痒评分(0.103[-0.831, 1.038])均有所改善。未发现安全问题。

结论

OTC 1%燕麦片乳膏在对症治疗儿童轻至中度AD方面与处方屏障乳膏同样有效且安全。

试验注册号

NCT01326910。

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