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临床试验/TCTR20200108001
TCTR20200108001尚未招募3 期

Effects of Dialysate/Replacement Supraphysiologic Sodium Concentration and Hemodynamic Stability in Critically-ill Patients receiving Continuous Renal Replacement Therapy (CRRT) : A Randomized, Double-blinded, Controlled Study

Division of Nephrology, Department of Internal Medicine, Faculty of Medicine0 个研究点目标入组 64 人开始时间: 2020年1月8日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
64

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 0 N/A (No limit)(—)
性别
All

入选标准

  • 1. Age of 18 years or more
  • 2. ICU patients requiring continuous renal replacement therapy
  • 3. Patients with adequate volume status assessed by inferior vena cava distensibility index <18 % or pulse pressure variation < 13 %
  • 4. Patients who are being on inotropic agents
  • 5. Patients or family members can provide consent

排除标准

  • 1. Patients with serum sodium levels <125 mmol/L
  • 2. Patients with mean arterial pressure <65 mmHg with adequate dose of inotropic agents
  • 3. Patients with severe acidosis (defined by blood pH <7.15)
  • 4. Pregnancy
  • 5. Uncontrolled bleeding

研究者

发起方
Division of Nephrology&#44; Department of Internal Medicine&#44; Faculty of Medicine

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