CTRI/2017/08/009582已完成4 期
A randomised, double blind, comparative clinical trial assessing the effectiveness and safety of dapsone 5% versus clindamycin 1% in the treatment of mild to moderate acne vulgaris - DCRCT
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 51
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.Subjects of 12 to 40 years of age of either sex
- •2.Mild to moderate acne: >= 2 but <= 30 total lesions - inflammatory (papules and pustules) and/or non-inflammatory (open and closed comedones)
- •3.Lesions in the face which correspond to a baseline investigator global assessment (IGA) score of 2 or 3
排除标准
- •1.Age <12 or >40
- •2.Total lesion count < 2 or >30,
- •3.Subjects regularly using any anti-acne medications in the last 30 days before study entry
- •4.Severe acne: Subjects with nodulo-cystic lesions, acne conglobata, acne fulminans
- •5.Pregnancy or intention of pregnancy and breastfeeding
- •6.Patients with G6PD deficiency
- •7.History of having taken any medication that could interact with dapsone (e.g. Trimetoprim-sulfametoxazol
- •8.Known hypersensitivity to the study medication
- •9.Patients not willing to comply with protocol requirements
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