跳至主要内容
临床试验/CTRI/2023/03/050912
CTRI/2023/03/050912尚未招募Unknown

Primary Objective: To evaluate the efficacy Skin Care Formulation in terms of Skin Brightening Effect on healthy female subjects. Secondary Objective: To evaluate the in-vivo safety and efficacy of a skin care formulation in terms of Improvement in Skin Water Barrier Function and in Skin Smoothness on healthy female subjects.

DPKA UNIVERSAL CONSUMER VENTURES PRIVATE LIMITED0 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 / Asian female subjects
  • 2.Healthy subjects (no infectious and evolutive pathology which could make the subject vulnerable
  • and stop the study, no pathology which could interfere with the study, no symptom in the process
  • of an exploratory checkup)
  • 3.Between 18 and 50 years of age
  • 4.Skin is healthy on the studied anatomic unit (free of eczema, wounds, inflammatory scarâ?¦.)
  • Specific criteria
  • 5.44 Subjects representing varied skin types (ideally equal representation of all 4 skin types â?? Oily,
  • Normal, Dry and Combination)+13 sensitive skin (declared through lactic acid sting test).
  • 6.Having wheatish to dark complexion.

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.Having a chronic dermatosis liable to modify the cutaneous reactivity on the tested area
  • 5.Being insulin-dependent diabetic or non insulin-dependent diabetic with a recent therapy (less
  • than 6 months)
  • 6.Having a progressive asthma (either under treatment or last fit in the last 2 years)
  • 7.Being epileptic
  • 8.Having non stabilized thyroid problems (requirement of a stabilized treatment for at least 6
  • 9Having cutaneous hypersensitivity
  • 10.Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic
  • products or food products or to latex
  • 11.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)
  • 12.Having undergone a surgery requiring a general anaesthetic of more than one hour in the past 6
  • 13.Having changed her cosmetic habits in the 14 days preceding the start of the study on the studied
  • anatomic unit
  • 14.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).
  • 15.Do not take part in any family planning activities leading to pregnancy and breastfeeding
  • 16.Do not take part in another study liable to interfere with this study
  • 17.Do not take 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)
  • 18.Do not change her cosmetic habits apart from the particular conditions mentioned in the protocol, on the studied anatomic unit
  • 19.During the study: Do not use other cosmetic products than the tested products to the studied areas (only usual cleanser/soap is accepted)
  • 20.The day of the measurements: No test product must be used (only face cleaned with water is
  • 21.Having started, changed or stopped a hormonal treatment (hormonal contraception, Hormone
  • Replacement Therapy) in the past 3 months.
  • 22.Having started, changed or stopped her tobacco consumption (for smokers consuming more than
  • 10 cigarettes per day) in the previous 6 months
  • 23.Having taken a medicinal treatment which could lead to hyper pigmentation (phenytoïn,
  • amiodarone, metals, minocyclineâ?¦) in the previous 6 months
  • 24.Taking oral supplements with major or minor effect on whitening of skin (e.g. vitamin C, beta￾
  • caroteneâ?¦)
  • 25.Having had beauty treatment (e.g. skin cleansing, exfoliation, scrub, mask â?¦) or having applied
  • self-tanning products in the week preceding the start of the study
  • 26.Having applied products with anti-wrinkle action (Retinoic acid, retinol, retinaldehyde,
  • isotretinoin, A.H.A...) in the 2 weeks preceding the start of the study
  • 27.Having applied products with a depigmenting action (hydroquinone or derivatesâ?¦) in the 4 weeks
  • preceding the start of the study.

研究者

发起方
DPKA UNIVERSAL CONSUMER VENTURES PRIVATE LIMITED

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