CTRI/2023/11/059370已完成Unknown
A Proof-of-Concept, Efficacy Study of Midnight Kohl Pencil for Long Lasting Effect in Healthy Adult Human Female Subjects. - Nil
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 入组人数
- 32
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.Age: 18 to 50 years (both inclusive) old at the time of consent.
- •2.Sex: Healthy human non-pregnant/non-lactating females.
- •3.Frequent user of kajal.
- •4.Females of childbearing potential must have a self-reported negative urine pregnancy test on Day 01 before application.
- •5.Subjects are generally in good general health as determined from recent medical history.
- •6.The subject does not have any previous history of adverse skin conditions and is not under any medication likely to interfere with the results.
- •7.The subject is willing and able to follow the study directions, participate in the study, returning for all specified visits.
- •8.The subject must be able to understand and provide written informed consent to participate in the study
排除标准
- •1.Subjects who are visually impaired or having underlying conditions that potentially impairs their vision.
- •2.Subject with eye makeup.
- •3.Subjects with known history of allergies or specific allergic reactions upon using ophthalmic cosmetic products.
- •4.Subjects with presenting ophthalmic conditions like dry eye, cataract, conjunctivitis etc.
- •5.Subjects who are regular users of prescription or cosmetic contact lens.
- •6.Subjects who have dark circles under their eyes.
- •7.Subjects who are reported pregnant/planning a pregnancy or lactating.
- •8.Subjects who are currently enrolled in an active investigational study or have participated in an investigational study within 30 days prior to enrolment.
- •9.Subjects, who in the opinion of the Investigator are not eligible for enrolment in the study.
研究者
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