NCT00366964已完成不适用
Determine The Efficacy Of The Wavelight Mydon Laser For Hair Removal And Treatment of Leg Veins
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 10
- 试验地点
- 2
- 主要终点
- Safety and efficacy of the treatment will determine the outcome.
研究概览
简要总结
This study is being done to compare the efficacy of an FDA cleared laser device with other similar systems in the market for the treatment of leg veins and hair removal in patients with darker skin type.
详细描述
The specific aim of the study is to determine the efficacy of this FDA approved laser for hair removal and treatment of leg veins in female patients having darker skin types (Fitzpatrick Skin type III-VI) and compare it with the efficacy of other similar commercial units available in the U.S.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Female patients of Asian and darker skin type greater than or equal to 18 years of age.
- •Ability to give informed consent.
排除标准
- •Taking medications that are photosensitizing.
- •History of skin disease in the area to be treated over the last 6 months.
- •Ongoing cutaneous lupus erythematosus, morphea, alopecia areata, or severe folliculitis.
- •History of keloidal or hypertrophic scarring.
- •Have inadequate hair growth in the test area of axilla.
- •Have unrealistic expectations of the treatment.
- •Co-existing severe emotional, medical or surgical illness leading to the inability to meet the follow-up requirements.
结局指标
主要结局
Safety and efficacy of the treatment will determine the outcome.
时间窗: 6 months
次要结局
未报告次要终点
研究者
研究点 (2)
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