CTRI/2011/091/000041已完成4 期
Assessment of Efficacy, Safety and Tolerability of D?acne (Clindamycin Phosphate 1% and zinc acetate) in the treatment of Acne.
Glenmark Pharmaceuticals Ltd0 个研究点目标入组 125 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 125
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Pms
入排标准
入选标准
- •?Subjects with mild to moderate inflammatory acne with comedones, papules or pustules predominate (Grade 1 and grade 2, IADVL acne grading system) affecting face
- •?Subjects must be 18-40 years of age
- •?Subjects must provide written informed consent and comply to the protocol
排除标准
- •?Subjects not willing to discontinue all topical treatments for Acne for 2 weeks prior to enrollment in study
- •?Hypersensitivity to any ingredients of D?acne
- •?Pregnant and lactating women.
- •?Subjects taking Concomitant therapy that might interfere with the study results in the investigator?s opinion.
- •?Subjects with dermatological disorder of face that may interfere with study evaluation.
研究者
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