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临床试验/CTRI/2026/03/106712
CTRI/2026/03/106712尚未招募不适用

To evaluate the safety and efficacy of skin care formulation in terms of skin hydration, skin water barrier, glow, firmness, elasticity, brightness and dark spots on healthy male and female subjects.

Bio Veda Farmacy Private Limited1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2026年3月31日
适应症
相关药物

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
36
试验地点
1
主要终点
skin hydration, skin water barrier, glow, firmness/elasticity, brightness, dark spots

研究概览

简要总结

OBJECTIVE·       Primary Objective

The objective of this study is to evaluate the safety and efficacy of skin care formulation in terms of skin hydration, skin water barrier, glow, firmness/elasticity, brightness, acne PIH spots, on healthy male and female subjects.

·       Secondary Objective

Secondary objective is to evaluate the in-vivo efficacy of a skin care formulation in terms of skin softness & smoothness, dark spot density, brightness, wrinkles, fine lines on healthy male and female subjects.

The evaluation will be performed using: Subject Self Evaluation (SSE), Dermatological Evaluation: Cosmetic Acceptability, Dermatological Evaluation: Efficacy, Chromametry, Tewametry, Corneometry, Glossymetry, Mexametry, Cutometry, Dino-lite, Antera 3D, Digital Photographs

POPULATION36 (18 males & 18 females) will be selected for the study.

The subjects selected for this study will be healthy male & females, aged between 25 and 50 years, having dull skin with visible wrinkles, fine lines,  and dark spots.

 STUDY DURATIONDuration: 28 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
25.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • 1.Indian male & female subjects 2.Healthy subjects 3.Skin is healthy on the studied anatomic unit 4.Having dull skin with visible wrinkles, fine lines, dark spot.

排除标准

  • 1 For female:- Being pregnant or breastfeeding or having stopped to breastfeed in the past three months 2 Having refused to give her assent by not 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 Having a chronic dermatosis liable to modify the cutaneous reactivity on the tested area (except for specific studies on a determined dermatosis) 7 Having non stabilized thyroid problems (requirement of a stabilized treatment for at least 6 months) 8 Being epileptic.
  • 9 Following a chronic medicinal treatment comprising any of the following products: aspirin-based products, anti-inflammatories, antihistamines, corticotherapy, taken by general or local routes (the only medication permitted is paracetamol) 10 Having cutaneous hypersensitivity.
  • 11 Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic products.
  • 12 Having undergone a surgery requiring a general anaesthetic of more than one hour in the past 6 months.

结局指标

主要结局

skin hydration, skin water barrier, glow, firmness/elasticity, brightness, dark spots

时间窗: Baseline, 30 minutes after application, 8 hours after application, Day 1, day 7, Day 14, Day 28

次要结局

  • skin softness & smoothness, dark spot density, brightness, wrinkles, fine lines(baseline, 30 minutes after application, 8 hours after application, Day 1, day 7, Day 14, Day 28)

研究者

发起方
Bio Veda Farmacy Private Limited
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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