The Effectiveness of a Novel Lip Product Containing Caulerpa Lentillifera Extract for Reducing Lip Hyperpigmentation
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Change from baseline in improving lip hyperpigmentation
研究概览
简要总结
The goal of this clinical trial is to evaluate the efficacy of the novel lip product containing Caulerpa lentillifera extract on the appearance and perception of dark lips in Thai adults aged 18 to 60 who report concerns about darkened lips. The main question it aims to answer is: Can the novel lip product containing C. lentillifera extract will significantly improve the appearance and perception of dark lips in Thai adults by reducing hyperpigmentation compared to baseline measurements?
Participants will apply the lip product twice a day, in the morning after breakfast and before bedtime, and refrain from using other lip products throughout the clinical trial period (7 days).
Researchers will compare the result to baseline measurements
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Understand the study protocol and provide informed consent after being informed of potential risks and benefits.
- •Refrain from using any other lip products, including lipstick, lip gloss, or lip conditioners, during the study period.
排除标准
- •Have a known allergy or sensitivity to cosmetic products or Caulerpa lentillifera.
- •Are on medication one month prior to study commencement.
- •Exhibit lip abnormalities such as malformation, inflammation, swelling, or sores.
研究组 & 干预措施
Lip product application group
干预措施: Lip product (Other)
结局指标
主要结局
Change from baseline in improving lip hyperpigmentation
时间窗: Baseline and 7 days
Lip hyperpigmentation is assessed using Antera3D at baseline and 7 day after usage
次要结局
- Change from baseline in improving lip dryness(Baseline and 7 days)
- Subjective assessment by participants(Baseline, day 1, and day 7)