跳至主要内容
临床试验/NCT03068156
NCT03068156已完成不适用

Efficacy of 308-nm Excimer Laser for Primary Localized Cutaneous Amyloidosis Treatment in Asians: Pilot Study

Chulalongkorn University1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2022年1月31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
入组人数
15
试验地点
1
主要终点
Roughness evaluation by using Visioscan® VC98

研究概览

简要总结

Efficacy of 308-nm excimer laser for primary localized cutaneous amyloidosis treatment in Asians, pilot study.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
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
All
接受健康志愿者
是

入选标准

  • •Patients, aged >18 years old with lichen amyloidosis diagnosed by using clinical presentation and pathologic features

排除标准

  • •Those with cutaneous amyloidosis associated systemic diseases
  • •Pregnancy or lactating woman
  • •Those who are allergic to urea, olive oil
  • •Those who are photosensitive to ultraviolet radiation
  • •Those who had been previously treated with medications/ radiation/ laser within 3 months for systemic and 1 month for topical therapy

研究组 & 干预措施

excimer laser

Experimental

干预措施: 308-nm excimer laser (Radiation)

Control

No Intervention

结局指标

主要结局

Roughness evaluation by using Visioscan® VC98

时间窗: Change from baseline roughness at every 2 weeks up to 16 weeks

The improvement of roughness evaluation

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Einapak Boontaveeyuwat, MD

Asst. Prof.

Chulalongkorn University

研究点 (1)

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