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
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