Jerajani Hr, Janaki C, Kumar Sharath, Phiske Meghana
Department of Dermatology, LTMM College and LTMG Hospital, Sion, Mumbai, India.
Indian J Dermatol. 2013 Jan;58(1):34-8. doi: 10.4103/0019-5154.105284.
Sertaconazole is a new, broad spectrum, fungicidal and fungistatic imidazole with added antipruritic and anti-inflammatory activity that would provide greater symptomatic relief and hence would be beneficial in improving the quality of life for the patient with dermatophytoses.
To compare efficacy and safety of sertaconazole, terbinafine and luliconazole in patients with dermatophytoses.
83 patients with tinea corporis and tinea cruris infections were enrolled in this multicentre, randomized, open label parallel study. The initial 'Treatment Phase' involved three groups receiving either sertaconazole 2% cream applied topically twice daily for four weeks, terbinafine 1% cream once daily for two weeks, luliconazole 1% cream once daily for two weeks. At the end of treatment phase, there was a 'Follow-up Phase' at end of 2 weeks, where the patients were assessed clinically and mycologically for relapse.
Of the 83 patients, 62 completed the study, sertaconazole (n = 20), terbinafine (n = 22) and luliconazole (n = 20). The primary efficacy variables including change in pruritus, erythema, vesicle, desquamation and mycological cure were significantly improved in all the three groups, as compared to baseline, in the Treatment and Follow-up phase. Greater proportion of patients in sertaconazole group (85%) showed resolution of pruritus as compared to terbinafine (54.6%); and luliconazole (70%), (P < 0.05 sertaconazole vs terbinafine). There was a greater reduction in mean total composite score (pruritus, erythema, vesicle and desquamation) in sertaconazole group (97.1%) as compared to terbinafine (91.2%) and luliconazole (92.9%). All groups showed equal negative mycological assessment without any relapses. All three study drugs were well tolerated. Only one patient in sertaconazole group withdrew from the study due to suspected allergic contact dermatitis.
Sertaconazole was better than terbinafine and luliconazole in relieving signs and symptoms during study and follow up period. At the end of 'Treatment Phase' and 'Follow-up' Phase, all patients showed negative mycological assessment in all three treatment groups suggesting no recurrence of the disease.
舍他康唑是一种新型的广谱咪唑类药物,兼具杀菌和抑菌作用,还具有止痒和抗炎活性,能更有效地缓解症状,从而有助于改善皮肤癣菌病患者的生活质量。
比较舍他康唑、特比萘芬和卢立康唑治疗皮肤癣菌病的疗效和安全性。
83例体癣和股癣患者参与了这项多中心、随机、开放标签的平行研究。初始“治疗阶段”包括三组,分别为:每日两次外用2%舍他康唑乳膏,持续四周;每日一次外用1%特比萘芬乳膏,持续两周;每日一次外用1%卢立康唑乳膏,持续两周。治疗阶段结束后,进入为期2周的“随访阶段”,对患者进行临床和真菌学复发评估。
83例患者中,62例完成了研究,其中舍他康唑组20例,特比萘芬组22例,卢立康唑组20例。在治疗和随访阶段,与基线相比,所有三组的主要疗效指标,包括瘙痒、红斑、水疱、脱屑的改善以及真菌学治愈情况均有显著改善。舍他康唑组(85%)瘙痒症状缓解的患者比例高于特比萘芬组(54.6%)和卢立康唑组(70%),(舍他康唑与特比萘芬相比,P < 0.05)。舍他康唑组平均总综合评分(瘙痒、红斑、水疱和脱屑)下降幅度(97.1%)大于特比萘芬组(91.2%)和卢立康唑组(92.9%)。所有组真菌学评估均为阴性,无复发情况。所有三种研究药物耐受性良好。舍他康唑组仅有1例患者因疑似过敏性接触性皮炎退出研究。
在研究和随访期间,舍他康唑在缓解体征和症状方面优于特比萘芬和卢立康唑。在“治疗阶段”和“随访阶段”结束时,所有三个治疗组的患者真菌学评估均为阴性,表明疾病无复发。