跳至主要内容
临床试验/NCT01691729
NCT01691729已完成不适用

A Randomized, Multicenter, Cross-Over Study Comparing the Performance of Three Ostomy Accessory Products

ConvaTec Inc.8 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2012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
ConvaTec Inc.
入组人数
26
试验地点
8
主要终点
Leakage & Wear Time

研究概览

简要总结

To purpose of the study is to evaluate and compare the efficacy of three ostomy accessory products.

详细描述

The primary objective of this study was to evaluate and compare the efficacy of three ostomy accessory products in terms of leakage and wear time. Secondary objectives were to evaluate and compare the safety of three ostomy accessory products, and to assess and compare the performance of the three products in terms of use and overall impression.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Double (Participant, Investigator)

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

  • Has an ostomy
  • Is at least 18 years of age
  • Has a stoma for at least 3 months
  • Other than thier ostomy is considered to have a healthy/stable health
  • Is able to take care of their stoma

排除标准

  • Known sensitivity to any of the ostomy devices or components
  • Is undergoing chemotherapy or radiotherapy
  • Has participated in a clinical study within the past 30 days
  • Has a medical condition, in which in the opinion of the Investigator would not be a good candidate for the study and justifies exclusion

结局指标

主要结局

Leakage & Wear Time

时间窗: 10 days

Evaluation and comparison of the efficacy of three ostomy accessory products in terms of leakage and wear time.

次要结局

  • Number of adverse events(10 days)

研究者

发起方
ConvaTec Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (8)

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