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硝酸舍他康唑 2%乳膏与咪康唑治疗皮肤皮肤癣菌病的疗效和耐受性比较。

Efficacy and tolerability of sertaconazole nitrate 2% cream vs. miconazole in patients with cutaneous dermatophytosis.

机构信息

Medical Services, Glenmark Pharmaceuticals Ltd, Mumbai, India.

出版信息

Mycoses. 2011 May;54(3):217-22. doi: 10.1111/j.1439-0507.2009.01801.x.

DOI:10.1111/j.1439-0507.2009.01801.x
PMID:19925567
Abstract

Sertaconazole is a new antifungal agent. To compare the efficacy and tolerability of sertaconazole and miconazole cream in cutaneous dermatophytosis, this prospective, randomized, multicentric comparative, phase 4 study was undertaken in 260 patients with cutaneous dermatophytosis after approvals from Institutional Ethics Committees. Patients were assigned to sertaconazole cream (2%) or miconazole cream (2%) topically twice daily for 2 weeks after obtaining informed consent. Efficacy variables included changes in mean scores of erythema, pruritus, desquamation, erythema/itching, burning/weeping, scaling/pustule and overall global assessment. Safety and tolerability were also assessed. A total of 122 patients in the sertaconazole group and 128 in the miconazole group completed the study with 10 drop-outs. There was a significant decrease (P < 0.05) in mean symptom scores and total scores from the first week onwards, sustained till 2 weeks and statistically significant (P < 0.05) in favour of sertaconazole. Moreover, 62.3% patients had complete clinical cure in the sertaconazole group (P < 0.05) compared with 44.6% in miconazole users. Both drugs were well tolerated and five patients in the sertaconazole group and nine in the miconazole group reported mild to moderate adverse events. Therapy with sertaconazole cream (2%) provided a better efficacy and tolerability compared with the miconazole cream (2%) and could thus be a therapeutic option in cutaneous dermatophytosis.

摘要

舍他康唑是一种新型抗真菌药物。为了比较舍他康唑和咪康唑乳膏治疗皮肤癣菌病的疗效和耐受性,在获得机构伦理委员会批准后,对 260 例皮肤癣菌病患者进行了这项前瞻性、随机、多中心、对照、4 期研究。患者在知情同意后,每天外用 2%舍他康唑乳膏或 2%咪康唑乳膏,每日 2 次,共 2 周。疗效变量包括红斑、瘙痒、脱屑、红斑/瘙痒、灼热/流泪、鳞屑/脓疱和总体全面评估的平均评分变化。还评估了安全性和耐受性。共有 122 例舍他康唑组和 128 例咪康唑组患者完成了研究,有 10 例脱落。从第 1 周开始,平均症状评分和总分均显著下降(P<0.05),持续至第 2 周,舍他康唑组有统计学意义(P<0.05)。此外,舍他康唑组 62.3%的患者完全临床治愈(P<0.05),而咪康唑组为 44.6%。两种药物均耐受良好,舍他康唑组有 5 例和咪康唑组有 9 例患者报告出现轻度至中度不良反应。与咪康唑乳膏(2%)相比,2%舍他康唑乳膏治疗皮肤癣菌病具有更好的疗效和耐受性,因此可能是一种治疗选择。

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