CTRI/2019/03/018139已完成4 期
CLINICAL STUDY TO EVALUATE THE EFFECTIVENESS OF A TEST FACE WASH FOR OILY SKINâ?? - EOCFW
Ramaiah Indic Specialty ayurveda restoration Hospital0 个研究点目标入组 50 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
- 50
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.Male and female volunteers, with age 18â??45 years
- •2.Subjects willing and able to provide informed consent voluntarily
- •3.with facial oiliness as assessed by Baumann skin oiliness scale (SOS) score of >=13
- •4.Willing to maintain the investigational product use throughout the study.
- •5.Subjects who have not undergone any skin therapy in last 3 months
- •6.Subjects with no known allergy to any of the test ingredients
- •7.Women using oral contraceptives must have been doing so for at least 6 consecutive months prior to entering the study, and are required to continue with the same brand throughout the study period
- •8.Subjects who are willing to refrain from using any skin care product other than the investigational product, like, moisturizers, face washes and face creams, for the duration of the study
- •9.Subjects willing and able to comply with all trial requirements
- •10. Laboratory workup within normal limits; including complete hemogram, glucose, blood urea nitrogen, creatinine, liver function test, lipid profile, thyroid-stimulating hormone, urine pregnancy test
排除标准
- •1.Subjects who have skin diseases like psoriasis, atopic dermatitis etc. at the time of screening
- •2.Subject with chronic systemic illnesses or treatment that can affect skin health eg. Polycystic ovarian disease
- •3.Subjects on oral medications or suffering from chronic illness which will compromise the study
- •4.Women who have stopped using oral contraceptives less than three months prior to entering the study
- •5.Subjects who have participated in a similar investigation in the past four weeks
- •6.Pregnant or lactating women
研究者
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