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临床试验/CTRI/2023/06/053620
CTRI/2023/06/053620已完成Unknown

Clinical Study to Assess Safety, Efficacy, & Short-Term ConsumerBenefits of Facial Clay Mask in Healthy Female Subjects

DPKA Universal Consumer Venture Private Limited0 个研究点目标入组 55 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
55

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) Age: 21 to 50 years (both inclusive) old at the time of consent.
  • 2) Sex: Healthy human non-pregnant/non-lactating females.
  • 3) Frequent users of international brands.
  • 4) Females of childbearing potential must have a self-reported negative urine pregnancy test.
  • 5) Subjects are generally in good general health as determined from recent medical history.
  • 6) The subject is willing and able to follow the study directions, participate in the study,
  • returning for all specified visits.
  • 7) The subject must be able to understand and provide written informed consent to participate
  • in the study.

排除标准

  • Subjects must not be enrolled in the study if they meet any one of the following criteria:
  • 1) Subject with known allergy or sensitization to cosmetic products.
  • 2) The subject has clinically significant skin disease, which may contraindicate participation,
  • including psoriasis, eczema, Skin cancer or other skin pathology.
  • 3) Medication which may affect skin response and/or past medical history.
  • 4) Individuals with active (flaring) disease or chronic skin allergies (atopic dermatitis/eczema)
  • or those who have recently undergone treatment for skin cancer (within the last 12 months)
  • in the area of testing on the forehead, nose and the cheeks.
  • 5) Female volunteers who have started a new hormonal birth control agent or switched to a
  • hormonal birth control agent within the past 60 days.
  • 6) Individuals who have had any medical or cosmetic procedure, such as laser resurfacing, or
  • plastic surgery to the test site (face) within the last 6 months. This includes botulinum toxin,
  • dermal fillers, collagen or other similar cosmetic procedure.
  • 7) Individuals who are currently using or during the past 14 days have used a retinoid such as
  • tretinoin, adapalene, or retinol containing agents or a hydroquinone containing agent.
  • 8) Individuals who have used mineral clay masks on their face within the last 14 days.
  • 9) Individuals who have been on any topical prescribed medications for the past 2 weeks.
  • 10) An individual who has a medical condition or is taking or has taken a medication which, in
  • the Investigator’s judgment, makes the subject ineligible or places the subject at undue
  • 11) Participation in other clinical studies simultaneously.

研究者

发起方
DPKA Universal Consumer Venture Private Limited

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