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临床试验/NCT04672993
NCT04672993已完成不适用

Exploratory Study of a New Urine Collection Device for Men

Coloplast A/S1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2020年11月2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
20
试验地点
1
主要终点
Percentage of Participants That Found the Product to be Comfortable to Wear

研究概览

简要总结

The aim of the investigation is to evaluate the subjects experience of a new collection device for men.

An open-labelled, single arm study design was chosen for this investigation with a duration of 1 week + up to 3 days extra.

研究设计

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

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
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 le-gal capacity
  • •Suffering from urinary incontinence equiva-lent to using up to 6 pads or 2 diapers per day
  • •Have had current incontinence issues for at least 3 months
  • •Able to understand patient information and able to change the product himself
  • •Up to 6 of the subjects can be users who are using an intermittent catheter due to re-tention, but who are also dribble inconti-nent in-between catheterizations, and hence need a product to handle the inconti-nence.
  • •Able to fit the test product.

排除标准

  • •If experiencing incontinence less than once per week
  • •Bedridden, using wheelchair or using a walking aids regularly

研究组 & 干预措施

Urine Collection Device for Men

Experimental

Test of Urine Collection Device for Men for 7 (+/- 3/0 days).

干预措施: Urine collection device for men (Device)

结局指标

主要结局

Percentage of Participants That Found the Product to be Comfortable to Wear

时间窗: One week

Questionnaire used to measure the frequency of success in support of "comfortable": "How comfortable was the product to wear?". The question was asked at the end of the trial.

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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