跳至主要内容
临床试验/NCT02886455
NCT02886455已完成不适用

Evaluation of the Influence of Output on Skin Covered by Newly Developed Adhesives

Coloplast A/S2 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2016年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Coloplast A/S
入组人数
4
试验地点
2
主要终点
Trans epidermal water loss

研究概览

简要总结

The study investigates the impact real output has on peristomal skin covered by a newly developed adhesive and a standard adhesive.

研究设计

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

入排标准

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

入选标准

  • Have given written informed consent
  • Be at least 18 years of age and have full legal capacity
  • Have had an ileostomy for more than one year
  • Have intact skin on the area used in the evaluation
  • Has an ileostomy with a diameter up to (≤) 35 mm
  • Have a peristomal area accessible for application of patches/adhesive strips (assessed by investigating scientist)

排除标准

  • Currently receiving or have within the past 2 month received radio- and/or chemotherapy
  • Currently receiving or have within the past month received topical steroid treatment in the peristomal skin area or systemic steroid (tablet/injection) treatment.
  • Are pregnant or breastfeeding
  • Having dermatological problems in the peristomal- or abdominal area (assessed by investigating scientist)
  • Participating in other interventional clinical investigations or have previously participated in this evaluation

结局指标

主要结局

Trans epidermal water loss

时间窗: 4-24 hours

The condition of the skin (transepidermal water loss) is measured after removing the adhesive by TE

次要结局

未报告次要终点

研究者

发起方
Coloplast A/S
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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