Kavli G, Larsen P O
Allergy. 1981 Nov;36(8):597-600. doi: 10.1111/j.1398-9995.1981.tb01877.x.
35 adult patients with atopic dermatitis were included in a double-blind crossover trial comparing chromone-2-carboxylic acid, FPL 57787 18 mg x 4, with placebo. Each treatment period lasted for 6 weeks with clinical assessment every 3 weeks. 28 patients completed 3 weeks of each period. Significant differences at the 5% level in favour of FPL 57787 were seen in the group starting on placebo. 17 patients completed the study. After 6 weeks there were no significant differences. 10 patients experienced dyspeptic side-effects. Further studies are warranted on clearly allergic sub-groups of atopic dermatitis patients.
35名成年特应性皮炎患者被纳入一项双盲交叉试验,该试验比较了色酮-2-羧酸、FPL 57787(18毫克×4)与安慰剂。每个治疗期持续6周,每3周进行一次临床评估。28名患者完成了每个阶段的3周治疗。在以安慰剂开始治疗的组中,在5%的水平上出现了有利于FPL 57787的显著差异。17名患者完成了研究。6周后没有显著差异。10名患者出现消化不良副作用。有必要对特应性皮炎患者中明确的过敏亚组进行进一步研究。