首页> 外文期刊>Current medical research and opinion >Efficacy of topical 10% urea-based lotion in patients with ichthyosis vulgaris: A two-center, randomized, controlled, single-blind, right-vs.-left study in comparison with standard glycerol-based emollient cream
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Efficacy of topical 10% urea-based lotion in patients with ichthyosis vulgaris: A two-center, randomized, controlled, single-blind, right-vs.-left study in comparison with standard glycerol-based emollient cream

机译:寻常性鱼鳞病患者局部用10%尿素基洗剂的功效:一项与标准甘油基润肤霜相比的两中心,随机,对照,单盲,右对左研究

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Background: Ichthyoses are genetic disorders of keratinization which are uncomfortable due to their conspicuous scaling, itching and cosmetic problems. Ichthyoses can lead to social discrimination and psychological problems. Ichthyosis vulgaris (IV) is the most common form of these geno-dermatoses. IV is a chronic disorder that often requires continuous therapy. Emollient and keratolytic products are the mainstay treatments of IV. It is important that efficient, safe and well tolerated therapies should be available. Direct comparative data regarding efficacy of different emollient products in IV patients are very few. Objective: The aim of the study was to investigate the keratolytic and moisturizing properties as well as the tolerance of a new urea topical formulation (Ureadin Rx10) when applied to hyperkeratotic and dry skin in patients with (IV) in comparison with a standard emollient cream. Methods: The study was conducted as a two-center, randomized, controlled, single-blind, intra-patient (right-vs.-left) trial design. A total of 30 patients with IV between 8 and 65 (mean age: 25 years) treated with a 10% urea-based lotion, Ureadin Rx 10** *Ureadin RX 10 is a registered trade name of ISDIN, Spain. (URx), for 4 weeks or a glycerol-based emollient cream, Dexeryl? ?Dexeryl is a registered trade name of Pierre Fabre Dermatologie. (DC), in a right-vs.-left study design. Primary outcome was a 5-point SRRC Index score (evaluating scaling roughness, redness and cracks) evaluated at baseline and after 2 and 4 weeks of treatment. As secondary endpoints patients evaluated also the global efficacy (GE) and global tolerability (GT) scores with the help of a 10cm visual analogue scale (0=no efficacy at all/very bad tolerability; 10: excellent efficacy/excellent tolerability). Results: At baseline the mean (SD) SRRC score was 9.5 (1.9) in the URx treated sites and 9.5 (1.9) in the DC treated sites. A total of 27 patients (90%) concluded the study period. Three patients were withdrawn prematurely because of itching and burning sensation after DC application (1 patient) or URx application (2 patients). At week 4, in comparison with baseline values, both treatments were shown to be clinically effective: SRRC significantly (p=0.0001) decreased to 3.3 (1.8) after URx (a 65% relative reduction) and to 5.7 (2.5) after DC (a 40% relative reduction). SRRC was significantly lower in URx treated regions in comparison with DC both after 2 and 4 weeks of treatment (p=0.0005). Mean GE score in areas treated with URx was significantly (p=0.0001) higher than in the areas treated with the DC (8.9 vs.7.3). Both treatments were in general well tolerated. GT score was 8.1 (range 10 to 3) with URx and 8.4 (range 10 to 3) with DC application (p=ns). The two main limitations of this trial are the study design (single blind), and the small sample size which is not adequate for an evaluation of safety. Conclusion: Ureadin Rx 10 lotion has shown a greater efficacy on ichthyosis vulgaris in term of reduction of scaling, roughness, redness and cracking in comparison with a glycerol-based emollient cream. Tolerability of the two topical treatments was comparable. Further studies with larger sample sizes are needed for the evaluation of safety and tolerability of urea 10% lotion in this clinical setting.
机译:背景:鱼鳞蛋白是角质化的遗传疾病,由于其明显的结垢,发痒和美容问题,因此不舒服。鱼鳞糖可导致社会歧视和心理问题。寻常鱼鳞病(IV)是这些基因皮肤病的最常见形式。 IV是一种慢性疾病,经常需要连续治疗。润肤和溶角蛋白产品是IV的主要治疗方法。重要的是应提供有效,安全且耐受良好的疗法。关于IV患者不同润肤剂功效的直接比较数据很少。目的:本研究的目的是与标准润肤霜相比,研究将新尿素外用制剂(Ureadin Rx10)应用于(IV)患者的高角化和干燥皮肤时的角质分解和保湿特性以及耐受性。方法:本研究以两中心,随机,对照,单盲,住院患者(右对左)试验设计进行。使用10%尿素基乳液Ureadin Rx 10 **治疗的30例IV年龄介于8至65岁(平均年龄:25岁)的患者* Ureadin RX 10是西班牙ISDIN的注册商标。 (URx),4周或甘油基润肤霜Dexeryl? ?Dexeryl是Pierre Fabre Dermatologie的注册商标。 (DC),在左右对比研究设计中。主要结果是在基线以及治疗2和4周后评估的5分SRRC指数评分(评估结垢粗糙度,发红和裂纹)。作为次要终点,患者还借助10厘米视觉模拟量表评估了总体疗效(GE)和总体耐受性(GT)评分(0 =完全没有疗效/非常差的耐受性; 10:优异的疗效/优异的耐受性)。结果:基线时,在URx处理部位的SRRC平均(SD)评分为9.5(1.9),在DC处理部位的SRRC评分为9.5(1.9)。共有27位患者(90%)结束了研究期。 3例患者因DC(1例)或URx(2例)施用后出现瘙痒和烧灼感而提前退出。在第4周,与基线值相比,两种治疗均显示出临床效果:SRRC(p = 0.0001)在URx后显着降低(3.3%(1.8%),相对降低65%),在DC后显着降低至5.7(2.5)(2.5%)。相对减少40%)。在治疗2周和4周后,与DC相比,URx治疗区域的SRRC显着降低(p = 0.0005)。用URx治疗的区域的平均GE评分显着(p = 0.0001)高于用DC治疗的区域(8.9 vs.7.3)。两种治疗一般都耐受良好。使用URx时,GT得分为8.1(范围10到3),使用DC时,GT得分为8.4(范围10到3)(p = ns)。该试验的两个主要局限性是研究设计(单盲)和样本量小,不足以评估安全性。结论:与甘油基润肤乳霜相比,Ureadin Rx 10乳液在减少鱼鳞病,减少结垢,粗糙,发红和破裂方面显示出对寻常性鱼鳞病的更大功效。两种局部治疗的耐受性相当。在此临床环境中,需要进行更大样本量的进一步研究,以评估10%尿素洗剂的安全性和耐受性。

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