CTRI/2024/01/061801尚未招募未知
A prospective, interventional, and multi-center study to characterize the efficacy and performance of the 100% Silicone Foley Balloon Catheter 2-way, 100% Silicone Foley Balloon Catheter – BH model 2-way, and 100% Silicone Foley Balloon Catheter – Star/ Ribbed model 2-way - nil
Sterimed Group0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.All subjects who undergo urinary catheterization indicated for long term catheterization of minimum of 30 days
- •2.Both Male and Female patients will be enrolled
- •3.All patients who are willing to provide informed consent for participation in the study
排除标准
- •1.Subjects not suitable for intervention with silicone Foley catheter
- •2.All subjects who are not willing to provide informed consent for participation in the study
- •3.Pediatric population
- •4.Neurogenic bladder condition subjects
- •5.Immobilized subjects
- •6.Subjects having urethral strictures
研究者
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