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临床试验/IRCT20201129049534N1
IRCT20201129049534N1已完成3 期

The effects of L-carnitine supplementation on inflammatory factors, oxidative stress and clinical outcomes in sepsis patients admitted to the intensive care unit (ICU): A double-blind randomized clinical controlled trial

Esfahan University of Medical Sciences0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
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

年龄范围
18 years 至 no limit(—)
性别
All

入选标准

  • Diagnosis of sepsis based on blood culture and approval of an ICU specialist and anesthesiologist and infectious disease specialist
  • Gastrointestinal with normal function and intestinal nutrition criteria
  • Accept informed consent

排除标准

  • Patient or family dissatisfaction
  • Patients who are hospitalized in the ICU for less than 48 hours or do not have the possibility of intestinal feeding and patients who receive nutritional support with full intravenous feeding
  • Patients who do not have an indication for intestinal nutrition on the first day and are confirmed and predicted based on the diagnosis of the intensive care unit that they will not be able to receive intestinal nutrition in the future. (Nausea, persistent vomiting, ileus, intestinal obstruction, uncontrolled diarrhea (> 500 ml per day), high-output fistula (> 500 ml per day), intestinal inaccessibility, incomplete resuscitation and hemodynamic instability
  • Cancer patients undergoing chemotherapy and taking cisplatin
  • Patients taking anticonvulsants (phenobarbital and phenytoin)
  • Patients taking pivalic acid, valproic acid and Ifosfamide
  • Patients taking levetiracetam
  • Patients undergoing dialysis
  • Patients with hyperthyroidism and hypothyroidism
  • Severe and progressive septic shock
  • Patients who are expected to die within 2 days of admission to the ICU
  • Patients with BMI<18.5 kg/m2 admitted to the IC

研究者

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