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临床试验/IRCT20190911044744N1
IRCT20190911044744N1招募中3 期

Comparison of the effect of silymarin and placebo on serum liver enzyme level in patients with trauma in the Intensive Care Unit in Rajaei hospital

Shiraz University of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
90

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
16 years 至 no limit(—)
性别
All

入选标准

  • People aged 16 or over
  • Not taking a known hepatotoxic drug
  • Not taking oral silymarin during the past day
  • No confirmed history of allergic reactions following oral administration of silymarin
  • Alanine aminotransferase (ALT) levels more than 2-fold above normal (> 70 IU / L) up to 4-fold above normal Or aspartate aminotransferase (AST) levels more than 2-fold above normal (> 70 IU / L) up to 4-fold above normal
  • Not taking concomitant antioxidants or compounds such as vitamin A, C, E and N-acetyl cysteine
  • Oral tolerance to medications

排除标准

  • Pregnancy or lactation
  • History of advanced liver disease

研究者

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