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临床试验/NCT02645773
NCT02645773已完成不适用

Early Intervention With Non-ablative Fractional Laser to Reduce Cutaneous Scarring

Bispebjerg Hospital1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2015年9月1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
16
试验地点
1
主要终点
To measure the clinical effect on scarring of non-ablative laser intervention at the three time-points

研究概览

简要总结

To investigate intervention with early application of non-ablative laser to prevent scarring in the skin

详细描述

To intervene in scar formation at three different time-points

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者
是

入选标准

  • •good health
  • •Skin type 2-3
  • •non-smokers
  • •presenting full medical record

排除标准

  • •active skin disease in test area
  • •resent UV-exposure in test area
  • •history of keloid
  • •current or resent cancer
  • •uncontrolled systemical disease

研究组 & 干预措施

Pre-laser

Experimental

non-ablative laser Laser Pre-wounding low dose laser Pre-wounding medium dose laser Pre-wounding high dose

干预措施: non-ablative laser (Device)

Immediate-laser

Experimental

non-ablative laser Laser low dose - immediate after wounding Laser medium dose - immediate after wounding Laser high dose - immediate after wounding

干预措施: non-ablative laser (Device)

Post-laser

Experimental

non-ablative laser Laser low dose - post wounding Laser medium dose - post wounding Laser medium dose - post wounding

干预措施: non-ablative laser (Device)

Control

No Intervention

Untreated control wound

结局指标

主要结局

To measure the clinical effect on scarring of non-ablative laser intervention at the three time-points

时间窗: 3 months after

Clinical evaluation by scar scales

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

Katrine Elisabeth Karmisholt

MD

Bispebjerg Hospital

研究点 (1)

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