跳至主要内容
临床试验/NCT05693948
NCT05693948已完成不适用

The Efficacy of Topical Serum X Containing Arbutin and Glutathione for Skin Brightening

Ungku Shahrin Medical Aesthetic Research & Innovation (USMARI) Centre1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2022年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
34
试验地点
1
主要终点
Changes in skin tone from baseline and at week 4, week 8, and week 12 after usage of serum X.

研究概览

简要总结

This study is conducted to evaluate the effectiveness of topical serum X containing arbutin and glutathione for skin brightening. The study duration is 12 weeks and the skin assessment will be carried out at baseline, week 4, 8 and week 12.The main questions this study aims to answer are:

  1. The skin brightening effect of the product on facial skin.
  2. To observe any adverse effect occurrence with the usage of the product.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 30 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Malaysia citizen
  • •Male and female (age 18-30 years old)

排除标准

  • •Participant with severe acne skin condition
  • •Participant who is taking isotretinoin, immunocompromised patients and received laser and light treatment within the last three months
  • •Participant who undergo whitening or cosmetic treatments such as botox and dermal fillers within the previous six month
  • •Participant with a history of facial surgery such as facelift or nose reshaping
  • •Participant with history of allergies to any ingredient in the study product
  • •Participant who is pregnant or plan to get pregnant

研究组 & 干预措施

Serum X

Experimental

Participants will used serum X twice daily for 12 weeks

干预措施: Other: Serum X (Other)

结局指标

主要结局

Changes in skin tone from baseline and at week 4, week 8, and week 12 after usage of serum X.

时间窗: Baseline and at week 4, week 8, and week 12

Skin tone will be assessed using JANUS III skin analyzer

Adverse effect after using serum X

时间窗: Week 12

Based on adverse effect occurrence on participants that occur during study period (12 weeks

次要结局

未报告次要终点

研究者

发起方
Ungku Shahrin Medical Aesthetic Research & Innovation (USMARI) Centre
申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验