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临床试验/TCTR20210122005
TCTR20210122005已完成4 期

Continuous vancomycin infusion versus intermittent infusion in critically ill patients

Faculty of Medicine Siriraj Hospital0 个研究点目标入组 31 人开始时间: 2021年1月22日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
31

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 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • 1. Adult patients (18 years old or over)
  • 2. Creatinine clearance (CrCl) by Cockcroft-Gault formula of more than 30 ml/min/1.73m2
  • 3. Had or was suspected of having Staphylococcal or Enterococcal infections
  • 4. Vancomycin was indicated and was anticipated for at least 48 hours.

排除标准

  • 1. History of receiving vancomycin within 48 hours before the study
  • 2. History of vancomycin allergy
  • 3. Pregnant or lactating woman
  • 4. Patient with acute kidney injury
  • 5. Body mass index below 15 kg/m2
  • 5. Receiving renal replacement therapy or extracorporeal membrane oxygenator
  • 6. The treating physician considers as inappropriate for continuous infusion.
  • 7. Do-not-resuscitation and terminally ill condition
  • 8. Denials the consent

研究者

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