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临床试验/NCT05931887
NCT05931887已完成不适用

Evaluation of the Novel Silq ClearTract Catheter in Patients With Chronic Urinary Retention

Silq Technologies Corporation1 个研究点 分布在 1 个国家目标入组 115 人开始时间: 2023年7月26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
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

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

Active Comparator

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

Active Comparator

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)

研究者

发起方
Silq Technologies Corporation
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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