跳至主要内容
临床试验/CTRI/2024/10/074760
CTRI/2024/10/074760已完成2 期

A study to evaluate the efficacy of test product in improving dark hair density

Hindustan Unilever Ltd1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2024年10月12日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
45
试验地点
1
主要终点
Improvement in dark hair density

研究概览

简要总结

This clinical trial is being conducted to ascertain the efficacy and safety of test product on healthy human Indian volunteers suffering from hair greying problems in their early age.

Volunteers will be enrolled basis on inclusion criteria mentioned in the protocol.

Product usage instruction will be provided to volunteers at the initiation of the study. Safety and efficacy assessment will be done by the experts at regular period as per protocol.

Assessment will be compared change form baseline value.

研究设计

研究类型
Interventional
分配方式
Na
盲法
Investigator Blinded

入排标准

年龄范围
20.00 Year(s) 至 42.00 Year(s)(—)
性别
All

入选标准

  • Participants having grey hair
  • Male and female participants
  • Participants in the age group 20-42 years (both the ages inclusive).
  • Participants willing to give a written informed consent and who agree to come for regular follow up visits.
  • Participants willing to trim their hair.
  • Participants willing to apply the test product as per instructions.

排除标准

  • Participant who are currently using henna/dye.
  • Participants using any hair product which impact hair colour will be excluded.
  • Participants who have taken chemotherapy for cancer in the 6 months prior to start of the study or have a plan to do treatments during study.
  • Female subjects who are pregnant or lactating (self-declared).
  • Participants who have had hair transplant.
  • Chronic illness which may influence the scalp condition.

结局指标

主要结局

Improvement in dark hair density

时间窗: 1 month, 2 month, 3 month, 4 month.

次要结局

  • NA(NA)

研究者

发起方
Hindustan Unilever Ltd
申办方类型
Other [fmcg]
责任方
Principal Investigator
主要研究者

Dr Mukta Sachdev

MS Clinical Research Pvt. Ltd

研究点 (1)

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