跳至主要内容
临床试验/NCT01957488
NCT01957488已完成不适用

Investigating the Safety and Performance of Two New 1-piece Ostomy Products in 180 Subjects With Ileostomy

Coloplast A/S8 个研究点 分布在 4 个国家目标入组 183 人开始时间: 2013年7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
183
试验地点
8
主要终点
Leakage

研究概览

简要总结

The aim of the current investigation is to investigate the performance of two new 1-piece ostomy products

详细描述

The present investigation aims at testing the performance and safety of the two new 1-piece ostomy products

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Supportive Care
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 and signed letter of authority (mandatory in DK)
  • Be at least 18 years of age and have full legal capacity.
  • Be able to handle the products themselves
  • Have an ileostomy with a diameter between 10 and 40 mm.
  • Have had their ostomy for at least three months.
  • Have within the last month used a 1-piece flat product with open bag
  • Currently using midi or maxi bags
  • Willing to use minimum 1 product every second day, i.e. maximum 2 days wear time.
  • Be suitable for participation in the investigation
  • Must be able to use custom cut product
  • Negative result of a pregnancy test for women of childbearing age (only DK)

排除标准

  • Currently receiving or have within the past 2 months received radio- and/or chemotherapy.
  • Currently receiving or have within the past month received systemic steroid or local treatment in the peristomal area
  • Are pregnant or breastfeeding
  • Participating in other interventional clinical investigations or have previously participated in this investigation
  • Has participated in the previous explorative Coloplast studies CP236 and CP237
  • Are currently or during the study using ostomy belt
  • Has a stoma below skin surface
  • Currently suffering from peristomal skin problems (i.e.bleeding and/or broken skin)
  • Has known hypersensitivity towards any of the test products

结局指标

主要结局

Leakage

时间窗: 14 +- 1 days

The fraction of baseplates with No leakage/seeping under the baseplate was measured. Leakage/seeping under the baseplate was assessed after each baseplate change.

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 (8)

Loading locations...

相似试验