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临床试验/CTRI/2026/03/105462
CTRI/2026/03/105462尚未招募不适用

To evaluate the in-vivo safety and efficacy of the skin care formulation in terms of reduction in pore appearance on healthy female subjects

Naturis Cosmetics Pvt. Ltd.1 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16日

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

研究概览

简要总结

OBJECTIVE :The objective of this study is to evaluate the in-vivo safety and efficacy of the skin care formulation in terms of reduction in pore appearance on healthy female subjects.The evaluation is performed using: Subject Self Evaluation (SSE)  , Dermatological Evaluation: Cosmetic Acceptability, Dermatological Evaluation: Efficacy, Chromametry, Digital Photographs

POPULATION : 36 Female subjects are selected for the study.. The subjects selected for this study are healthy females, aged between 18 and 35 years, having pores.STUDY DURATION :  28 days following the first application of the regime.

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
18.00 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 visible pores on skin.

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 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.

研究者

发起方
Naturis 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)

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