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临床试验/CTRI/2026/01/101062
CTRI/2026/01/101062尚未招募不适用

To evaluate the in vivo safety and efficacy of a skin care formulation in terms of its efficacy to reduce tanning and to improve the skin brightness on healthy female subjects

Idam Natural Welness pvt. ltd.1 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2026年1月24日

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
33
试验地点
1

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 a skin care formulation in terms of its efficacy to reduce tanning and to improve the skin brightnesson healthy female subjects

The evaluation is performed using:Subject Self Evaluation, Dermatological Evaluation: Cosmetic Acceptability, Chromametry

 POPULATION : 33 female subjects are selected for the study.

The subjects selected for this study are healthy females aged between 20 and 35 years, having Dull skin.

 STUDY DURATION : 3 days following the first application of the product.

研究设计

研究类型
Interventional
分配方式
Na
盲法
Participant and Outcome Assessor Blinded

入排标准

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

入选标准

  • 1.Indian Female subjects 2.Healthy subjects 3.Skin is healthy on the studied anatomic unit 4.Having dull skin.

排除标准

  • Being pregnant or breastfeeding or having stopped to breastfeed in the past three months.
  • Having refused to give his/her assent by not signing the consent form.
  • Taking part in another study liable to interfere with this study.
  • Being diabetic.
  • Being asthmatic.
  • 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 (except in the case of studies with evaluation of sensitive skin).
  • Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic products.
  • Having undergone a surgery requiring a general anesthesia of more than one hour in the past 6 months.
  • Having changed his/her cosmetic habits in the 14 days preceding the start of the study on the studied anatomic unit.

研究者

发起方
Idam Natural Welness pvt. ltd.
申办方类型
Other [Personal Care or Beauty Industry]
责任方
Principal Investigator
主要研究者

Dr Niharika Salian

MASCOT-SPINCONTROL India Pvt. Ltd.

研究点 (1)

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