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临床试验/CTRI/2023/10/058546
CTRI/2023/10/058546尚未招募2 期

Comparison of outcome in Terlipressin and ultra-low dose Terlipressin plus noradrenalin infusion in HRS-AKI patients of ACLF - NI

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试验速览

阶段
2 期
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

  • ACLF as per APASL criteria
  • AKI at admission as defined by ICA-AKI criteria
  • HRS-AKI grade II & grade III as defined by ICA 12 hour of admission

排除标准

  • Age <18 years >70 years
  • Septic shock
  • Patient with HCC outside Milan’s criteria
  • Severe Hyponatremia (Na <120 MEq/L)
  • Patients with RH failure, CAD, PVD, arrhythmias and cardiomyopathy
  • Pregnancy or Lactating mother
  • Grade III/IV HE or Shock requiring inotropes or patients on mechanical ventilator at time of randomization
  • In-hospital new AKI
  • Active urinary sediments – 2+ albumin or above, dysmorphic RBCs
  • Known CKD, obstructive uropathy
  • Lack of informed consent
  • Prior intolerance or S/E to Terlipressin or albumin

研究者

发起方
on sponsered

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