跳至主要内容
临床试验/NL-OMON52449
NL-OMON52449招募中4 期

Revised dosing recommendations of ciprofloxacin for patients with impaired renal function: a bioequivalence study. - Revised dosing recommendations of ciprofloxacin

Academisch Medisch Centrum0 个研究点目标入组 58 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
入组人数
58

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
18 至 99(—)

入选标准

  • - being treated with ciprofloxacin intravenously (iv) or orally (po) as part of
  • standard care
  • - age >= 18 years
  • - being admitted to general wards of the Amsterdam UMC - location AMC, the
  • OLVG- location Oost or Noordwest Ziekenhuisgroep location Alkmaar
  • - informed consent is obtained

排除标准

  • - receiving renal replacement therapy (i.e. haemodialysis, peritoneal dialysis,
  • continuous venovenous hemofiltration or another way of renal replacement
  • therapy), during the first 48 hours of treatment with ciprofloxacin
  • - patients with cystic fibrosis (CF)
  • - informed consent is not obtained

研究者

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