CTRI/2023/03/050735已完成2 期
A prospective, open label, one arm clinical study to evaluate the safety and efficacy of Retractable Kohl Kajal in healthy female volunteers
Sunshine Industries0 个研究点目标入组 20 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 20
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.Female subjects between the age group of 18 to 50 years.
- •2.Subjects who are able to give written informed consent and ready to comply with the protocol.
- •3.Subjects who are regular users of kajal or eye liner
排除标准
- •1.Subjects who are visually impaired or having underlying conditions that potentially impairs their vision.
- •2.Subjects with known history of allergies or specific allergic reactions upon using ophthalmic cosmetic products.
- •3.Subjects with presenting ophthalmic conditions like dry eye, cataract, conjunctivitis etc.
- •4.Subjects who are regular users of prescription or cosmetic contact lens.
- •5.Subjects who have dark circles under their eyes.
- •6.Subjects who are reported pregnant/planning a pregnancy or lactating.
- •7.Subjects who are currently enrolled in an active investigational study or have participated in an investigational study within 30 days prior to enrolment.
- •8.Subjects, who in the opinion of the Investigator or the Expert Dermatologist are not eligible for enrolment in the study.
研究者
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