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临床试验/CTRI/2019/02/017813
CTRI/2019/02/017813已完成未知

Comparing the safety and efficacy of Amphotericin B deoxycholate continuous infusion for 24 hrs vs 4 hrs in trauma ICU.

Deptt of Anaesthesiology0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
60

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

  • Patients aged between 18 to 60 years with culture-based candida infection, having baseline Potassium, Creatinine, Liver Enzymes, and Urine Output within normal limits.

排除标准

  • Patients not giving consent,
  • Known case of allergy, hypersensitivity to AmpB deoxycholate,
  • History of any systemic illness,
  • Patients with deranged RFT and electrolyte imbalance,
  • patient on any other antifungal treatment.

研究者

发起方
Deptt of Anaesthesiology

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