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临床试验/NCT01018589
NCT01018589已完成2 期

Effect the Cicatrix Cream in in Treatment of Post Surgical Scars and and Epidermic Burn.

Catalysis SL2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2009年9月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
Catalysis SL
入组人数
100
试验地点
2
主要终点
Reduction of the areas of lesions at 2 months (end of the treatment)

研究概览

简要总结

The purpose of the study is to assess the effect of CICATRIX (Asian Gotu Kola or Pennywort) usage in the treatment of epidermic burns or post surgical scars. The duration of this phase 2 clinical trial will be two months.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
— 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patient with lesions characteristic of the investigated illness.
  • Signed informed consent

排除标准

  • Patient that refer manifestations of high sensibility to the medication or to some of the components of the product
  • Patient that don't want to participate in the study
  • Patient not very cooperative
  • Family responsible not very cooperative

结局指标

主要结局

Reduction of the areas of lesions at 2 months (end of the treatment)

时间窗: 2 months

次要结局

  • Coloration of the lesions at 2 months (end of the treatment)(2 months)
  • Adverse effects(2 months)

研究者

发起方
Catalysis SL
申办方类型
Industry

研究点 (2)

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