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Efficacy and safety of 1% terbinafine hydrochloride versus 2% sertaconazole cream in the treatment of tinea corporis

机译:1%盐酸特比萘芬与2%舍他康唑乳膏治疗体癣的疗效和安全性

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Background: Tinea corporis is a common superficial dermatophytosis seen in tropical countries. This study was done to compare the efficacy and safety of topical antifungal agents, terbinafine versus sertaconazole in the treatment of tinea corporis. Methods: This study was conducted in Babuji Hospital and Chigateri Government Hospital, Davangere. A total of 60 (n=60) patients were included and divided into two groups of 30 patients each in the study. 1st group - received topical 1% terbinafine hydrochloride and 2nd group - received 2% sertaconazole cream. Patients were advised to apply cream twice daily for 4 weeks. Improvement in clinical parameters like erythema, scaling, itching, and potassium hydroxide (KOH) mount were taken for assessing the efficacy of drugs. They were followed-up at the end of 2, 4, and 6 weeks to assess the improvement of the condition. Complete cure rate was defined as mycological cure with a complete absence of clinical signs and symptoms. For safety data of both drugs presence of any local side effects (like stinging sensation, swelling and increased erythema) were analyzed in both groups. Statistical analysis was done using students paired t-test and unpaired t-test. Results: When two groups were compared at the end of 2 weeks, complete cure rate for terbinafine was 80% as compared to 63.3% for sertaconazole (p at the end of 4 weeks, sertaconazole was as effective as terbinafine and statistically non-significant (p>0.05) results were obtained. KOH mount was negative in both groups at the end of 2nd week. Local side effects like erythema, swelling, stinging sensation were not noticed during the study in both the groups. Conclusion: From this study, it was shown that 2% sertaconazole cream was as effective as 1% terbinafine cream, though 1% terbinafine had higher rates of complete cure at the end of 2 weeks as compared to sertaconazole.
机译:背景:体癣是热带国家常见的浅表皮肤癣菌病。这项研究的目的是比较局部抗真菌药特比萘芬与舍他康唑治疗体癣的功效和安全性。方法:本研究在达沃格勒(Davangere)的Babuji医院和Chigateri政府医院进行。研究共纳入60名患者(n = 60),分为两组,每组30名患者。第一组-接受局部1%盐酸特比萘芬,第二组-接受2%舍他康唑乳膏。建议患者每天两次使用乳霜,持续4周。改善了红斑,脱屑,瘙痒和氢氧化钾(KOH)含量等临床参数,以评估药物的疗效。他们在第2、4和6周结束时进行了随访,以评估病情的改善。完全治愈率定义为完全没有临床体征和症状的真菌治疗。为了获得两种药物的安全性数据,分析了两组中是否存在任何局部副作用(如刺痛感,肿胀和红斑增加)。使用学生配对t检验和非配对t检验进行统计分析。结果:当在2周结束时比较两组时,特比萘芬的完全治愈率为80%,而舍他康唑为63.3%(4周末的p,舍他康唑与特比萘芬一样有效,在统计学上无统计学意义( p> 0.05)结果,两组在第2周结束时KOH呈阴性,两组均未观察到局部副作用,如红斑,肿胀,刺痛感。结果表明,与舍他康唑相比,2%舍他康唑乳膏与1%特比萘芬乳膏一样有效,尽管1%特比萘芬在2周末的完全治愈率更高。

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