Grigoriu D, Grigoriu A
Dermatologica. 1983;166 Suppl 1:8-13. doi: 10.1159/000249908.
A total of 61 patients with proven fungal infection of the skin or with erythrasma took part in a double-blind comparison of the efficacy, toleration and safety of tioconazole base 1% w/w and econazole nitrate 1% creams applied twice daily. Some patients had more than one site of infection and some were infected with more than one fungal/bacterial species. The mean duration of treatment in the tioconazole group of patients was 40 days (range: 12-68) and in the econazole group 38 days (range: 17-101). Clinical and mycologic cure was achieved in 27 of 29 (93.1%) tioconazole-treated and 29 of 31 (93.5%) econazole-treated patients. All but 1 of the cured patients in each treatment group were seen some 6 weeks after the end of treatment; all remained clinically and mycologically cured. Both creams were found to be generally acceptable in terms of ease of application. Some staining was reported in both treatment groups. One side effect of mild intermittent pruritus was reported in an econazole-treated patient. The minimum inhibitory concentrations were determined.
共有61例确诊为皮肤真菌感染或患有红癣的患者参与了一项双盲试验,比较1%w/w的噻康唑基质乳膏和1%硝酸益康唑乳膏每日两次外用的疗效、耐受性和安全性。一些患者有不止一处感染部位,还有一些患者感染了不止一种真菌/细菌。噻康唑组患者的平均治疗时长为40天(范围:12 - 68天),硝酸益康唑组为38天(范围:17 - 101天)。29例接受噻康唑治疗的患者中有27例(93.1%)实现了临床和真菌学治愈,31例接受硝酸益康唑治疗的患者中有29例(93.5%)实现了临床和真菌学治愈。每个治疗组中除1例治愈患者外,其余患者均在治疗结束约6周后接受观察;所有患者在临床和真菌学方面均保持治愈状态。两种乳膏在使用便利性方面总体上均可接受。两个治疗组均有染色报告。一名接受硝酸益康唑治疗的患者报告了轻度间歇性瘙痒这一副作用。测定了最低抑菌浓度。