NCT06336135已完成不适用
A Prospective, Single-blind, Randomized, Placebo-controlled, Clinical Trial Evaluating Reduction in Severity and Duration of Symptoms After Laser Therapy With Acorn aHFS
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 11
- 试验地点
- 1
- 主要终点
- Reduction in severity and duration of symptoms
研究概览
简要总结
This study evaluates the severity and duration of symptoms experienced after laser therapy comparing four post-procedure topical products. Each product is applied to an individual region of interest (5 cm diameter) on the back or décolleté according to randomization code after laser therapy. The subject, blind to the product applied to each of 4 regions of interest, assesses eight symptoms daily for 14 days. Photography is performed daily.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
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
- •Male or Female
- •Age: ≥18 and ≤60 years
- •Any skin tone Fitzpatrick score 1-2 (light), 3-4 (medium), 5-6 (dark)
- •Competent and willing to provide written, informed consent to participate in all study activities
排除标准
- •Pregnant women
- •Are participating/have participated in another interventional clinical trial in the last 30 days which may confound the results of this study, unless approved by Sponsor
- •Use of retinoids 7 days prior to the procedure
- •Active cutaneous infections in the treatment area
- •Diseases that could inhibit healing, such as scleroderma, or other cutaneous conditions that could confound study results
- •Subjects unable to communicate with the investigator and staff
- •Any health condition that in the investigator's opinion should preclude participation in this study
结局指标
主要结局
Reduction in severity and duration of symptoms
时间窗: 2 weeks
Each region of interest will be evaluated daily for the severity and duration of eight symptoms
次要结局
未报告次要终点
研究者
研究点 (1)
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