Evaluation of the Novel Silq ClearTract Catheter in Patients With Chronic Urinary Retention
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 115
- 试验地点
- 1
- 主要终点
- Number of Catheter Related Complications
研究概览
简要总结
To assess the ability of the Silq ClearTract™ 100% Silicone 2-Way Foley Catheter to reduce catheter associated complications in subjects that require a long-term indwelling Foley catheter when compared to other commercially available Foley catheters.
详细描述
A prospective, randomized, multi-center, post-market study in subjects that require a long-term indwelling Foley catheter.
Neurogenic bladder is commonly managed with indwelling catheters (urethral or suprapubic). Indwelling catheters are associated with multiple complications, including recurrent urinary tract infections and catheter obstruction. A randomly assigned catheter will be inserted using standard techniques. The assigned catheters will either be the SILQ ClearTract 100% Silicone 2-Way Foley Catheter or the current standard of care catheter. Subjects will continue to use the assigned catheter for a period of approximately 3 months following regular standard of care. Subjects will then be assigned the alternative catheter for an additional 3 month period after which they will be exited from the study
The purpose of the study is to compare the incidence of catheter-related complications between the SILQ treated catheter and the current standard of care catheter(s). Because these complications lead to more frequent interventions and associated treatment costs, the study will also calculate the economic impact of the use of SILQ treated catheters compared to standard of care catheters. Patient-reported outcomes will also be measured via questionnaires upon each study visit. Explanted catheter samples will also be sent to a core lab for quantification of the calcification present on the catheter surface.
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
- 是
入选标准
- •At least 18 years old
- •Requirement of a 14 Fr, 16Fr, or 18Fr indwelling urethral or suprapubic urinary catheter (for at least 6 months) for bladder drainage.
- •Able and willing to comply with study procedures
- •Able and willing to give informed consent.
排除标准
- •History of reconstructive bladder surgery such as bladder augmentation or continent catheterizable stoma.
- •Cognitive deficit limiting the ability to respond to clinical questionnaires.
- •Allergy or sensitivity to any catheter material used in this study.
研究组 & 干预措施
SILQ ClearTract 100% Silicone 2-Way Foley Catheter
Subjects in this arm will receive the SILQ ClearTract 100% Silicone 2-Way Foley Catheter for approximately the first 3 month period of enrollment. In a subsequent period of approximately 3 months subjects in this arm will receive their current standard of care catheter.
干预措施: SILQ ClearTract 100% Silicone 2-Way Foley Catheter (Device)
Standard of Care Catheter
Subjects in this arm will receive their current Standard of Care Catheter for the first 3 month period of enrollment. In a subsequent period of approximately 3 months subjects in this arm will receive the SILQ ClearTract 100% Silicone 2-Way Foley Catheter
干预措施: SILQ ClearTract 100% Silicone 2-Way Foley Catheter (Device)
结局指标
主要结局
Number of Catheter Related Complications
时间窗: 6 months
Catheter Related Complications can be classified as: i. Symptomatic Catheter Associated Urinary Tract Infection ii. Catheter Blockage iii. General Premature Interventions: Patient sought care for a catheter-related issue prior to their scheduled catheter exchange
次要结局
- Catheter Encrustation(6 months)
- Patient Preference(4 months)
- Catheter Related Complication Treatment Costs(6 months)
- Patient Satisfaction(6 months)
