跳至主要内容
临床试验/CTRI/2025/09/095326
CTRI/2025/09/095326
尚未招募
不适用

To evaluate and compare the in vivo safety and efficacy of skin care formulation versus untreated control in terms of moisturization, skin softness, glow and smoothness on healthy Human subjects

ClayCo. Cosmetics Pvt. Ltd.1 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2025年9月30日

概览

阶段
不适用
状态
尚未招募
发起方
ClayCo. Cosmetics Pvt. Ltd.
入组人数
33
试验地点
1
主要终点
Skin moisturisation, skin softness, glow and smoothness

概览

简要总结

OBJECTIVE: The objective of this study will be to evaluate and compare the in-vivo safety and efficacy of Skin Care  Formulation versus Untreated Control in terms of moisturisation, skin softness, glow and smoothness on healthy Human subjects for product coded:          The evaluation will be performed using:Subject Self Evaluation (SSE) , Dermatological Evaluation: Cosmetic Acceptability, Dermatological Evaluation: Efficacy, Corneometry

 POPULATION: 33 (17/16 Females & 16/17 Males) Subjects (30 completed cases) will be selected for the study.The subjects selected for this study will be healthy females aged between 18 and 40 years, having dry skin on forearm.

 STUDY DURATION:  24 hours following the first application of the product.

研究设计

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

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
All

入选标准

  • 1.Indian or Asian Male & Female subjects 2.Healthy subjects 3.Skin is healthy on the studied anatomic unit 4.Subject having dry skin type.

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.

结局指标

主要结局

Skin moisturisation, skin softness, glow and smoothness

时间窗: Baseline, 30 minutes, 4 hours, 24 hours after product application

次要结局

未报告次要终点

研究者

发起方
ClayCo. Cosmetics 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)

Loading locations...

相似试验