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临床试验/NL-OMON33557
NL-OMON33557招募中不适用

The contribution of glutamine to citrulline and arginine synthesis, when alanyl-glutamine is supplied in an enteral dose of 0.5 g/kg, in critically ill patients. - Dipep human IC

Vrije Universiteit Medisch Centrum0 个研究点目标入组 20 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
20

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 至 99(—)

入选标准

  • *Age: > 18 and < 80 years
  • *BMI > 18,5 and < 35
  • *Ability to tolerate enteral nutrition, provided by postpyloric tube, meeting full protein/energy requirements based on indirect calorimetric measurements
  • *Expected ICU or medium care stay of a minimum of 5 days
  • *Any ICU patient who is considered *stable*:
  • * Hemodynamics: no new vasoactive medication during 24 hrs preceding inclusion, maximum dose of vasoactive medication < 5 mg/kg/min
  • * Respiration: PaO2/FiO2 ratio > 200, PEEP < 15 cm H2O, when on respiration
  • *Having obtained his/her or his/her legal representative*s informed consent

排除标准

  • * Admission after elective surgery
  • * Pregnancy
  • * Liver failure, defined by bilirubin levels > 100
  • * Kidney failure, represented by increase in serum creatinine levels to > 100 umol/l, in the absence of primary underlying renal disease, or oliguria, defined as urine output < 20 ml/hour in the previous 6 weeks
  • * Urea cycle defects
  • * Chronic corticosteroids use ( > 7. mg/ day > 3 weeks)
  • * Bowel malabsorption possibly interfering with intestinal absorptive function, e.g. celiac disease, crohn*s disease, presence of fistulas, major intestinal malabsorption disorder, or short bowel syndrome
  • * Parenteral feeding
  • * Use of medium chain triglycerides or glutamine/citrulline supplements

研究者

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