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临床试验/ACTRN12610000147088
ACTRN12610000147088已完成4 期

A Randomized, Blinded, Multicentre Non-inferiority Study Comparing the Acid-base Effects of Plasmalyte and Hartmann’s solution in Patients undergoing Liver Resection

Austin Hospital0 个研究点目标入组 50 人开始时间: 2010年2月12日最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Adult patients having elective liver resection surgery

排除标准

  • 1. Patient declines to take part
  • 2. Age less than 18 years
  • 3. Abnormal pre-operative coagulopathy: INR (international normalised ratio) > 1.4, platelet count < 75 x 109/l
  • 4. Severe hepatic insufficiency (bilirubin > 30umol/L, ALP (alkaline phosphatase) >300iu/L, ALT (alanine transaminase) > 50iu/L, albumin < 25g/dL, INR > 1.5
  • 5. Moderate/severe renal impairment: serum creatinine > 200ummol/l
  • 6. Hyperkalaemia (serum potassium > 5.6)
  • 7. American Society of Anaesthesiologists (ASA) physical status IV or V
  • 7. Patients with a known previous allergic reaction to study solutions

研究者

发起方
Austin Hospital

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