首页> 外文期刊>Clinical, Cosmetic and Investigational Dermatology >Efficacy of a Topical Product Containing Purified Omental Lipids and Three Anti-Itching Compounds in the Treatment of Chronic Pruritus/Prurigo Nodularis in Elderly Subjects: A Prospective, Assessor-Blinded, 4-Week Trial with Transepidermal Water Loss and Optical Coherence Tomography Assessments
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Efficacy of a Topical Product Containing Purified Omental Lipids and Three Anti-Itching Compounds in the Treatment of Chronic Pruritus/Prurigo Nodularis in Elderly Subjects: A Prospective, Assessor-Blinded, 4-Week Trial with Transepidermal Water Loss and Optical Coherence Tomography Assessments

机译:含有纯化的题脂的疗效和三种抗瘙痒化合物在老年人的慢性瘙痒/普里氏菌结节中的治疗:一项前瞻性,评估杂乱,4周试验,具有Transepidermal水损和光学相干性断层扫描评估

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Purpose:To investigate the efficacy of a cream containing purified omental lipids 10% and three anti-itching substances (polidocanol/stimutex/palmitoylethanolamine) in elderly subjects with chronic pruritus/prurigo nodularis (CP/CPN).Patients and Methods:Thirty-five subjects (6 men; mean age 67±4 years) with CP/CPN were enrolled in a prospective, assessor-blinded, 4-week study. The cream was applied twice daily in the most affected body area. The primary endpoints were the evolution of the 10-cm visual analogue itch severity scale (VAS) and the 4-point verbal itching rating scale (VRS) (from 0 to 3). Secondary endpoints were the evolution of optical coherence tomography (OTC) of four skin parameters (acanthosis/hyperkeratosis/scale/dermal vascular pattern), assessed in a target lesioned area, and the transepidermal water loss (TEWL). Study endpoints were evaluated at baseline and after 2 and 4 weeks by an investigator unaware of the type of treatment.Results:All the enrolled subjects concluded the trial. At baseline, the mean±SD scores for VAS and VRS were 4.9±2.2 and 1.7±0.7, respectively. The treatment was associated with a significant reduction (p=0.0001) of VAS score of 60% at week 2 and of 86% at week 4. VRS score was significantly reduced by 49% after 2 weeks and by 81% after 4 weeks, in comparison with baseline. TEWL (expressed as g/m2/h) mean values were 18±5.4 at baseline and 12.7±4.4 at week 2 and 9.8±4.7 at week 4 (P=0.0001 vs baseline). All the OCT parameters evaluated improved during active treatment; acanthosis grade was 0.22 mm at baseline, 0.19 mm at week 2 and 0.17 mm at week 4 (p=0.0005), representing a 23% reduction in comparison with baseline. The product was very well tolerated.Conclusion:This purified omental lipid with three anti-itching components cream reduces significantly itch intensity in subjects with chronic pruritus/prurigo nodularis, improving the skin barrier function and skin structure.Trial Number:ISRCTN869561669.? 2020 Ardigò et al.
机译:目的:探讨含有纯化的蛋乳10%和三种抗瘙痒物质(Polidocanol /刺激/棕榈酰乙醇胺)在慢性瘙痒/普里氏菌(CP / CPN)中的老年受试者(CP / CPN)的疗效.Patiant和方法:三十五受试者(6人;平均年龄67±4年),CP / CPN注册了一个预期,评估别盲,4周的研究。在受影响最大的体积中每天涂上两次奶油。主要终点是10cm视觉模拟瘙痒严重性秤(VAS)的演变,4点言语瘙痒额定秤(VRS)(从0到3)。次要终点是四种皮肤参数的光学相干断层扫描(OTC)的演变(髋关节区/高穴/尺度/真皮血管图案),在靶损伤区域中评估,以及Transepidermal水分损失(Tewl)。研究终点是在基线中评估的,并通过调查员不知道治疗类型的调查员在2和4周后进行评估。结果:所有注册的科目都结束了审判。在基线时,VAS和VRS的平均值±SD分数分别为4.9±2.2和1.7±0.7。在第2周,第2周,第4周,第4周,第2周,第4周后,该治疗与60%的显着减少(p = 0.0001)的VAS得分为60%,vrs评分明显减少49%,4周后81%与基线的比较。 TEWL(表达为G / M2 / h)平均值为基线为18±5.4,第2周的第2周和9.8±4.4的12.7±4.4(P = 0.0001 VS基线)。所有OCT参数在主动处理期间评估的改善;基线的敏感级为0.22mm,每周2.19毫米,第4周的0.19毫米(P = 0.0005),与基线相比,减少23%。该产物耐受良好。结论:这种纯化的题脂,具有三种抗瘙痒组分霜,可在慢性瘙痒/普里氏核桃粒子的受试者中降低显着的瘙痒强度,改善皮肤屏障功能和皮肤结构。图数:ISRCTN8695616669。? 2020Ardigō等人。

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