Hyperkeratotic chronic tinea pedis treated with neticonazole cream

Ryoji Tsuboi, Tadahiko Matsumoto, Hideoki Ogawa, N. Kuriya, T. Yoshiike, C. Nishiyama, S. Arase, Y. Asada, N. Fujimoto, M. Fukuda, T. Fukumoto, T. Hamada, H. Horinosono, T. Horio, M. Ichihashi, T. Iida, M. Ikeda, I. Ishido, U. Iwasawa, K. KawahiraM. Kawashima, H. Kobayashi, H. Kodama, M. Mihara, M. Nagashima, M. Nagayama, K. Nakagawa, T. Natsume, Y. Nishikawa, T. Shiohara, T. Shirai, H. Suzuki, H. Takemura, E. Tanabe, A. Taneda, T. Tsuji, K. Uchida, M. Ueda, K. Unno, Y. Urano, R. Urashima, M. Utsunomiya, K. Yamamoto, Y. Yamashina

研究成果: Article査読

5 被引用数 (Scopus)

抄録

A total of 126 patients with tinea pedis were entered into this 4-week study of neticonazole (SS Pharmaceutical Co. Ltd., Tokyo), a new imidazole derivative recently developed and launched in Japan as a topical antifungal agent applied either with or without occlusive dressing. Diagnosis of the hyperkeratotic form of tinea pedis was established by a positive KOH wet mount and by clinical signs. Dermatophyte culture was performed from a designated target lesion before initiation of treatment. The patients, randomly assigned through a telephone service, were treated by neticonazole 1% cream once daily with either simple application (SA) or overnight occlusive dressing (ODT). Clinical improvements in the five clinical signs: pruritus, erythema, hyperkeratosis, fissure, and scale were assessed by the following criteria: marked improvement, moderate improvement, slight improvement, no change, and worsening. The mycologic response (KOH) and improvement of clinical signs of the two groups were evaluated 2 and 4 weeks after commencing treatment.

本文言語English
ページ(範囲)371-373
ページ数3
ジャーナルInternational Journal of Dermatology
35
5
DOI
出版ステータスPublished - 5月 1996

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