跳至主要内容
临床试验/CTRI/2023/03/050735
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

发起方
Sunshine Industries

相似试验