CTRI/2018/03/012727已完成未知
An open, prospective, randomized comparative study to assess the efficacy and safety of DRF/AY/5003 with a marketed drug in various conditions.
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 86
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 either sex in the age group of 16-30 yrs mild to moderate acne
- •2 Subjects who signed informed consent form.
- •3 Subjects with ability to comply with all study requirements.
- •4 Subjects free of Diabetes and any other clinically significant diseases .
- •5 Subjects with normal Liver Function Tests and Renal Function Tests
排除标准
- •1 Subjects with severe acne vulgaris who require anti-infective therapies.
- •2 Subjects suffering from acne congloblata, endocrinal and other systemic
- •3 Subjects with a lot of facial hair.
- •4 Pregnant or lactating mothers.
- •5 Subjects with involvement in any concurrent study, the nature of which may
- •affect the parameters being investigated in the study.
研究者
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