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临床试验/NL-OMON54700
NL-OMON54700招募中不适用

Single use vs reusable catheters in intermittent CatheterizatiOn for treatment of urinary retention: a Multicenter, Prospective, RandomizEd controlled, non-inferiority trial (COMPaRE) - COMPaRE

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 386 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
386

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

年龄范围
16 至 99(—)

入选标准

  • In order to be eligible to participate in this study, a subject must meet all
  • of the following criteria:
  • - Male/Female patients >= 16 years old.
  • - Diagnosed with urinary retention or significant post-void residue due to
  • non-neurogenic or neurogenic causes.
  • - Expected chronic, but at least for a duration of twelve months, necessity for
  • daily drainage of the urinary bladder.
  • - Be able to administer self CIC via the urethra daily and have at least two
  • weeks of experience in CIC.

排除标准

  • A potential subject who meets any of the following criteria will be excluded
  • from participation in this study: - Age < 16 years. - Temporary use of
  • catheterization because of transient causes. - Known significant urethral
  • stricture which prevents CIC. - Urinary tract stones. - Bladder augmentation. -
  • Non-urethral catheterization. - History of bladder cancer with active
  • follow-up. - The use of immunosuppressives for transplantation or auto-immune
  • diseases. - Neurocognitive disease which prevents complete comprehension of the

研究者

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