CTRI/2019/11/021907尚未招募4 期
A Randomized,Open label,Parallel group study to evaluate efficacy and safety of topical Eberconazole versus topical Terbinafine in Tinea versicolor
Dr Nidarsan Viswanathan0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1)age of patient more than 18 years
- •2)patient is willing and able to provide written informed consent
- •3)patient having a clinical diagnosis of Tinea versicolor with lesions occupying less than 10% body surface area on face,neck,upper chest and upper back.
- •4)patients having tinea versicolor confirmed by microscopic KOH test.
排除标准
- •1)patient age less than 18 years
- •2)Pregnant and lactating females patients
- •3)patients with all other types of tinea infections
- •4)patients having history of intolerance or hypersensitivity to study drugs
- •5)patients who had recieved systemic or topical antifungal treatment within one month.
- •6)patients with serious concomitant illness which could prevent completion of study
- •7)Patients who has extensive involvement with tinea versicolor and patients with contact dermatitis,atopic dermatitis,psoriasis or other skin diseases.
- •8)patient is unwilling or unable to sign the informed consent
- •9)patients who are taking immunosuppressive drugs.
研究者
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