Van Eygen M, Dils F, Gillerot J, Verschueren E
Eur J Pediatr. 1979 Jun 28;131(3):147-53. doi: 10.1007/BF00538939.
Levamisole was tested double-blind in 106 children with recurrent upper respiratory tract infections. They received either levamisole (n = 53) or placebo (n = 53) 0.5 ml/kg bodyweight b.i.d. for two consecutive days each week for six months. A control examination was performed every two months. Both groups were compared by means of the Fisher-test and the Mann-Whitney U-test (two-tailed probability each). Improvement was observed more frequently in the levamisole group with regard to the number of episodes of infection, and the total duration and severity of the infections. No side-effects, except for some stomach complaints in one levamisole patient, were reported.
对106名复发性上呼吸道感染儿童进行了左旋咪唑双盲试验。他们每周连续两天接受左旋咪唑(n = 53)或安慰剂(n = 53),剂量为0.5 ml/kg体重,每日两次,共六个月。每两个月进行一次对照检查。两组通过Fisher检验和Mann-Whitney U检验(双侧概率)进行比较。在感染发作次数、感染的总持续时间和严重程度方面,左旋咪唑组观察到更频繁的改善。除了一名左旋咪唑患者有一些胃部不适外,未报告有副作用。