CTRI/2017/12/010907已完成2 期
To evaluate the efficacy of hair removing cream formulations for hair.
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 23
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 in generally good health
- •2.Subjects in the age group of 18-35 years.
- •3.Subjects with moderate hair growth on lower outer forearms.
- •4.Subjects without any cuts, marks and open wounds on lower outer forearms.
- •5.Subject has not participated in a similar investigation in the past four weeks.
- •6.Subjects have not used a similar product for the last four weeks.
- •7.Subjects willing to give a written informed consent and come for regular follow up.
排除标准
- •1.Subjects with known allergies or sensitivities to cosmetic products, toiletries or its components like fragrances, preservatives,hydroquinone, vitamin C, Niacin amide,retinol, soy etc.
- •2.Currently or has been using topical retinoids, alpha-hydroxy and/or beta-hydroxy acids,hydroquinone or any whitening/Fairness preparation in any form (cleanser, toner, cream
- •or soaps) within the last 1 month.
- •3.Currently or has been undergoing dermatologist skin treatments or procedures within the last 1 month.
- •4.Currently or has been involved in another skin care clinical investigation within the last 3 months.
- •5.Subjects who have pre-existing or dormant dermatologic conditions (e.g., psoriasis,
- •rosacea, rashes, eczema, many and/or severe excoriations etc.) that could interfere with
- •the outcome of the study as determined by the investigator.
- •6.Subjects with scars which could interfere with expert grader and/or instrumental
- •evaluations.
- •7.Subjects who are nursing as determined by the investigator interview during screening or
- •pregnant as determined by the Urine pregnancy testing after screening.
- •8.Subjects viewed by the investigator as not being able to complete the study.
研究者
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