A Non-Inferiority Bladder Scan Study to Investigate Residual Urine After Use of Intermittent Catheters in Male Subjects
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 37
- 试验地点
- 1
- 主要终点
- Mean Residual Urine Volume
研究概览
简要总结
Male intermittent catheters (ICs) range from 340-500 mm long, with the European standard minimum length being 360 mm for a catheter without a balloon and 275 mm for one with a balloon. This length is defined by hospital standards although it is known that the male urethra has an approximate maximum length of 29 cmA new intermittent catheter developed by Coloplast A/S is a 30-cm-long sterile, ready-to-use, hydrophilic-coated male catheter. There is a lack of clinical data documenting that male ICs that are shorter and more or less flexible than standard catheters can sufficiently empty the bladder of male subjects. This will be tested using ultrasound to measure residual urine in the bladder following catheterisation with new product and standard length catheter.
详细描述
See brief summary
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
- Triple (Participant, Investigator, Outcomes Assessor)
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
- •Subject is a male IC user able to self-catheterise
- •Subject has used hydrophilic-coated ICs for at least 1 month
- •Subject is at least 18 years old.
- •Subject has provided informed consent.
排除标准
- •Subject has symptoms of UTI (ie, fever, autonomic dysreflexia, spasticity, discomfort or pain over the kidney or bladder, onset/increase in incontinence episodes, cloudy urine with increased odour, malaise, lethargy, or sense of unease).
- •Subject has known abnormalities in the lower urinary tract.
研究组 & 干预措施
SpeediCath catheter
Standard treatment
干预措施: SpeediCath (Device)
Test product
干预措施: Test Catheter - SpeediCath Compact Male (Device)
结局指标
主要结局
Mean Residual Urine Volume
时间窗: 3 catheterisations on 1 day
Residual urine was mesured by ultrasound measurement of bladder content after intermittent catherisation
次要结局
- The Difference in Incidence of Adverse Events (AEs) and Adverse Device Events (ADEs)(Study period)
- Median Absolute RU Volume(3 catheterisations on 1 day)
