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临床试验/NCT03044262
NCT03044262已完成不适用

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

Coloplast A/S1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2017年1月9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
发起方
Coloplast A/S
入组人数
15
试验地点
1
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
否

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

研究组 & 干预措施

Cohort 7

Experimental

This is a sub-study testing the effect of real output applied under two adhesive strips (standard adhesive strip and new adhesive strip) on the skin after 8 hours.

干预措施: Standard adhesive strip (Other)

Cohort 7

Experimental

This is a sub-study testing the effect of real output applied under two adhesive strips (standard adhesive strip and new adhesive strip) on the skin after 8 hours.

干预措施: New adhesive strip (Other)

结局指标

主要结局

Trans epidermal water loss

时间窗: 8 hours

The condition of the skin (trans epidemeral water loss) is measured after removing the adhesive.

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 (1)

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