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临床试验/IRCT20180404039187N2
IRCT20180404039187N2已完成3 期

study the effects of Allopurinol on liver enzymes and grade of fatty liver on ultrasound in patients with non-alcoholic fatty liver disease

Tabriz University of Medical Sciences0 个研究点目标入组 100 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
100

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 65 years(—)
性别
All

入选标准

  • patients whom have non-alcoholic fatty liver disease based on the ultrasound and laboratory tests
  • patients whom have non-symptomatic hyperuricemia (serum uric acid >7 mg/dl for men and >6.5 mg/dl for women)

排除标准

  • pregnancy and lactation
  • allergy to Allopurinol or its contents
  • use of alcohol
  • patients with renal deficiency with creatinine clearance (GFR) <30 mg/ml
  • simultaneous use of drugs which have interaction with Allopurinol (mercaptopurine, azathioprine, ...)
  • patients who have had gout or who are using uricosuric agents or thiazide diuretics

研究者

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