Prospective, Multi-Center, Randomized Study to Assess the Ability of the Silq ClearTract™ Urinary Catheter to Reduce Biofilm Formation When Compared to Two Types of Commercially Available Foley Catheters (Silver-Coated Latex and Silicone-coated Latex)
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 158
- 试验地点
- 8
- 主要终点
- Biofilm formation
研究概览
简要总结
To assess the ability of the Silq ClearTract™ 100% Silicone 2-Way Foley Catheter to reduce biofilm formation in subjects that require a long-term indwelling Foley catheter when compared to other commercially available urinary catheters.
详细描述
A prospective, randomized, multi-center, post-market study in subjects that require a long-term indwelling Foley catheter.
A randomly assigned catheter will be inserted using standard techniques. Non-surgical subjects will rate the level of pain associated with the insertion procedure using the visual analog scale (VAS). A urine sample will be collected immediately after catheter insertion, in order to generate a baseline urinalysis and urine culture.
Follow-up visits will be performed on Day 28, or upon catheter removal, whichever occurs first. The catheter will be removed on Day 28 or earlier if clinically indicated. The removed catheter will be processed and sent to the core laboratory for analysis. Urine will be collected immediately prior to catheter removal in order to conduct urinalysis and urine culture. Subject will rate level of pain associated with the removal procedure using the VAS. The subject will also fill out a questionnaire about their experience with the catheterization immediately after catheter removal. Subjects will then be exited from the study.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female age ≥ 18 years old;
- •Requiring indwelling 16Fr Foley catheter for at least 7 days;
- •Able and willing to comply with study procedure; and,
- •Able and willing to give informed consent.
排除标准
- •Allergy or sensitivity to any catheter materials used in this study;
- •Known urethral stricture which, in the opinion of the investigator, could influence the subject's evaluation of the catheter;
- •Planned Prophylactic use of antibiotics for CAUTI or any other infection beyond day 1 of the study (catheter implantation);
- •Symptomatic UTI being treated with antibiotics (as determined by the study PI, including at least one of the following: fever, chills, headache, burning sensation, burning of urethra or genital area, blood in urine, foul smelling urine and ≥ 10,000 cfu/mL);
- •Any other infection being treated with antibiotics at the time of catheter implantation;
- •Subjects requiring bladder irrigation during the study (an active voiding trial in surgical subjects prior to catheter removal is allowed);
- •Currently enrolled in another interventional clinical trial;
- •Any other condition that, in the opinion of the investigator, precludes study participation or poses a significant hazard in case of study participation; and
- •Females who are pregnant or breastfeeding or who plan to become pregnant during the study.
研究组 & 干预措施
Silq ClearTract™ 100% Silicone 2-Way Foley Catheter
Up to 82 subjects
干预措施: Long-term indwelling Foley catheter (Device)
Silver-coated Latex 2-Way Foley Catheter
Up to 82 subjects
干预措施: Long-term indwelling Foley catheter (Device)
Silicone-coated Latex 2-Way Foley catheter
Up to 82 subjects
干预措施: Long-term indwelling Foley catheter (Device)
结局指标
主要结局
Biofilm formation
时间窗: 5 to 7 days
A core lab will use the BacTiter-Glo Microbial Cell Viability Assay, a well characterized method for quantifying active biomass and biofilm, to determine biofilm formation on explanted catheter samples.
次要结局
未报告次要终点