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临床试验/CTRI/2023/02/049473
CTRI/2023/02/049473尚未招募未知

Comparison of efficacy, safety, pharmacokinetic and pharmacodynamic parameters between conventional dosing regimen of vancomycin with novel optimized dosing regimen in critically ill patients.

Prof Nusrat Shafiq0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

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

入选标准

  • Critically ill adults admitted to intensive care unit or emergency ward where intravenous vancomycin therapy is deemed necessary based on suspected or confirmed infectious aetiology.

排除标准

  • Patients less than 18 years.
  • Patients requiring renal replacement therapy.
  • Patients with end stage renal disease.
  • Patients with end stage hepatic failure.
  • Any contraindication or history of hypersensitivity with use of vancomycin.
  • Pregnant and lactating women.

研究者

发起方
Prof Nusrat Shafiq

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