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临床试验/NL-OMON45287
NL-OMON45287已完成不适用

Patient comfort assessment of the Femflow. A follow-up study of the validation of a new catheter for intermittent Self-Catheterization in female patients - Patient comfort assessment of the Femflow

ovuqare BV0 个研究点目标入组 10 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
已完成
发起方
入组人数
10

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 64(—)

入选标准

  • - Age 18-80 years
  • - Woman on CIC who cannot empty the bladder themselves (so no incomplete voiders)
  • - Patient has signed a written Informed Consent form
  • - Patient is free of uncontrolled psychiatric illness
  • - Patient is free of urinary tract infection
  • - is the patient free of urethral strictures, trauma of necrosis?

排除标准

  • - Patients with large deviations in urethra or bladder caused by anatomical defects, earlier surgery or caused by other damage of the pelvic floor.
  • - Patients with a urinary tract infection, or a history of urinary tract infections.
  • - Patients who can urinate themselves, or on partial Clean Intermittent Catheterization
  • - Morbid obesity (BMI > 40 kg/m2)
  • - Patients with hematuria and/or blood clots in the urine

研究者

发起方
ovuqare BV

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