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临床试验/IRCT2015010420514N2
IRCT2015010420514N2已完成3 期

Comparison of efficacy and safety of axilla hair reduction using ALX handpiece of MeDioStar NeXTPRO and Cynosure devices.

ational Institute for Medical Research Development (NIMAD)0 个研究点目标入组 20 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 years 至 50 years(—)
性别
All

入选标准

  • males or females with age of 18 – 50 years old; skin types II – IV; the subject must be willing to consent to participate in the study.
  • Exclusion criteria: children and pregnant or lactating women; any previous laser; treatment to the study areas; regional electrolysis within 6 months of study entry; history of keloid scarring; hormonal dysfunction; active cutaneous infection within the treatment area; chronic sun exposure or tanning; photosensitivity; use of medication with androgenic effects; history of skin pigmentation disorders; cancerous and pre-cancerous lesions in the treatment area; haired nevi in the treatment area; tattoos in the area to be treated.

排除标准

  • 未提供

研究者

发起方
ational Institute for Medical Research Development (NIMAD)

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