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临床试验/NL-OMON54617
NL-OMON54617招募中不适用

Antibiotic exposure at the infection site in periprosthetic joint infections - ASTERICS

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 120 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
120

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

  • - Age >= 18 years.
  • - Written informed consent has been obtained from the patient or their legally
  • authorized representative.
  • - Suffering from periprosthetic (hip or knee) joint infections and therefore
  • treated with one of the following antibiotics as part of the one-stage wo-stage
  • arthroplasty exchange:
  • IV: vancomycin, flucloxacillin or cefuroxime
  • Oral: flucloxacillin, clindamycin or co-trimoxazole or ciprofloxacine
  • - Patients undergoing a two-stage implant exchange of hip or knee with or
  • without antibiotic free interval prior to re-implantation.
  • - Able and willing to undergo joint punctures and venous blood sampling during
  • and, in case of an antibiotic free interval, at the end of the six-weeks
  • antibiotic treatment.

排除标准

  • - Unable to draw samples for study purposes; Except when a patient received a
  • vancomycin-loaded spacer, then they will remain included.
  • - Language barriers.
  • - The use of the target antibiotics at the start of study participation (and
  • therefore at the start of the antibiotic treatment as part of the two-stage
  • arthroplasty exchange).
  • - The use of drugs interacting with the target antibiotics.

研究者

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Antibiotic exposure at the infection site in... | 临床试验