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临床试验/CTRI/2024/08/072405
CTRI/2024/08/072405尚未招募不适用

To evaluate the in-vivo safety and efficacy of Hair care formulation in terms of reduction in hair fall on healthy female subjects

Deys Medical Stores Pvt Ltd1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2024年8月19日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
36
试验地点
1
主要终点
Reduction in hair fall

研究概览

简要总结

OBJECTIVE

The objective of this study will be to evaluate the in-vivo safety and efficacy of Hair care formulation

in terms of reduction in hair fall on healthy female subjects

The evaluation will be performed using:Subject’s Self Evaluation, Dermatological Evaluation: Cosmetic Acceptability, Counting of fallen hair after standardized combing

 The study lasts 42 days including the 14 days conditioning phase and 28 days treatment phase.

POPULATION:36 Female Subjects (30 Completed Cases) will be selected for the study.

The subjects selected for this study will be healthy females, aged between 18 and 35 years,

having moderate to severe hair fall.

研究设计

研究类型
Interventional
分配方式
Na
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 35.00 Year(s)(—)
性别
Female

入选标准

  • 1.Asian Indian female subjects.
  • 2.Healthy subjects 3.Skin is healthy on the studied anatomic unit (free of eczema, wounds, inflammatory scar….) 4.Having moderate to severe hair fall.

排除标准

  • Being pregnant or breastfeeding or having stopped to breastfeed in the past three months
  • Having refused to give her/his assent by not signing the consent form
  • Taking part in another study liable to interfere with this study
  • Being insulin-dependent diabetic or non-insulin-dependent diabetic with a recent therapy (less than 6 months)
  • Having a progressive asthma (either under treatment or last fit in the last 2 years)
  • Having a chronic dermatosis liable to modify the cutaneous reactivity on the tested area (except for specific studies on a determined dermatosis)
  • Having non stabilized thyroid problems (requirement of a stabilized treatment for at least 6 months)
  • Being epileptic.
  • Following a chronic medicinal treatment comprising any of the following products: aspirin-based products, anti-inflammatories, anti-histamines, corticotherapy, taken by general or local routes (the only medication permitted is paracetamol)
  • Having cutaneous hypersensitivity.
  • Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic products.

结局指标

主要结局

Reduction in hair fall

时间窗: Baseline , Day14, Day28

次要结局

未报告次要终点

研究者

发起方
Deys Medical Stores Pvt Ltd
申办方类型
Other [fmcg]
责任方
Principal Investigator
主要研究者

Dr Pooja Yadav

MASCOT-SPINCONTROL India Pvt. Ltd.

研究点 (1)

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