跳至主要内容
临床试验/CTRI/2017/12/010907
CTRI/2017/12/010907已完成2 期

To evaluate the efficacy of hair removing cream formulations for hair.

Dabur India Ltd0 个研究点目标入组 23 人开始时间: 待定最近更新:

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

相似试验