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临床试验/CTRI/2024/02/062693
CTRI/2024/02/062693尚未招募Unknown

PRIMARY OBJECTIVE: To evaluate and compare the in-vivo efficacy and safety of two skin regimes in terms of reduction in dark spots (Lightens the pigmentation of selected dark spots-age spots), improvement in skin moisturization upto 48 hours, improvement in skin brightening , improvement in skin firmness, elasticity, skin radiance, skin glow, skin softness, prevention of water loss from skin (TEWL parameter) and tan reduction, reduction in fine line and wrinkles and clear skin in terms of reduction in dark spot and on healthy female subjects.SECONDARY OBJECTIVE: To evaluate the subject feedback for product efficacy in terms of clear skin (basis reduction in dark spots) - NI

Incnut Lifestyle Retail Pvt Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方

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)Indian female subjects
  • 2)Having dry skin.
  • 3)Having normal skin type with Age Related Dark Spots.
  • 4)Having dull and tanned skin.

排除标准

  • 1)Being pregnant or breastfeeding or having stopped to
  • breastfeed in the past three months.
  • 2)Having refused to give her
  • assent by signing the consent form.
  • 3)Taking part in another study liable to interfere with this study.
  • 4)Being insulin-dependent diabetic or non insulin-dependent diabetic
  • with a recent therapy (less than 6 months)
  • 5)Having a progressive asthma (either under treatment or last fit in
  • the last 2 years)
  • 6)Being epileptic
  • 7)Having non stabilized thyroid problems (requirement of a stabilized
  • treatment for at least 6 months)
  • 8)Having cutaneous hypersensitivity
  • 9)Having a diagnosed or highly probable allergy to one or several
  • compounds of the cosmetic products or food products or to latex
  • 10) 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)
  • 11)Having undergone a surgery requiring a general anaesthetic of
  • more than one hour in the past 6 months.
  • 12)Having changed her cosmetic habits in the 14 days preceding the
  • start of the study on the studied anatomic unit
  • 13)Having applied a cosmetic product (included make-up) on the
  • studied areas the first day of the study (only face cleaned with water
  • is accepted).

研究者

发起方
Incnut Lifestyle Retail Pvt Ltd

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