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临床试验/NL-OMON50420
NL-OMON50420招募中不适用

Optimizing the treatment of cystitis using nitrofurantoin - FIRE

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 60 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
60

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 99(—)

入选标准

  • 1. Patients having been prescribed nitrofurantoin by treating physician because
  • suspicion of or proven urinary tract infection.
  • 2. Age of at least 18 years.
  • 3. Female sex
  • 4. Glomerular filtration rate (GFR) greater than or equal to 30 ml/min based on
  • creatinine clearance.
  • 5. Written informed consent by patient or legal representative

排除标准

  • 1. Treated with any antibiotics within 1 week of potential sampling period.
  • 2. Known porphyria
  • 3. Known allergic reaction or anaphylactic shock as a result of the consumption
  • of nitrofurantoin

研究者

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