跳至主要内容
临床试验/KCT0002729
KCT0002729招募中未知

The efficacy of carnitine complex(The efficacy of carnitine complex(GODEX ? R ) for the patients with moderate alcoholic liver disease: a multicenter, randomized, double blind, phase ? study

Kangdong Sacred Heart Hospital0 个研究点目标入组 38 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
38

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
20(Year) 至 o Limit(—)
性别
All

入选标准

  • 1.Over 19 years of age
  • 2.Individual who consume alcohol more than 40g per day for men and 20g for women
  • 3.Individual who has ADUIT K score over than 20 for men and 10 for women
  • 4.Individual who has their ALT and AST level above than normal range.
  • 5.40 IU/L =ALT, AST= 400 IU/L and AST/ALT= 1
  • 6.Individual who has their GGT level above than normal range.
  • 7.- GGT ; Men > 71 IU/L, Women > 42 IU/

排除标准

  • 1.Individual who has allergic response to Investigational product
  • 2.Parkinson’s disease patients who are taking Levodopa for treatment
  • 3.Individual who has Maddrey discriminant function score above 32
  • 4.Individual with Portal hypertension complications
  • 5.Individual with hepatorenal syndrome
  • 6.Individual with viral liver diseases, hepatocellular Carcinoma, liver disease from drug-taking or other liver disease which can affect the results of trial.
  • 7.Individual who experienced bacterial hepatitis in recent 6 months
  • 8.Individual with pancreatitis and HIV
  • 9.Individual with cardiac insufficiency, ischemic cardiomyopathy, respiratory failure
  • 10.Individuals who are taking Psychotropic medication except antidepressant
  • 11.Pregnant women, lactating women
  • 12.Individuals who are considered unsuitable by investigators due to other reasons
  • 13.Individual who didn’t consent with Investigator Consent Form
  • 14.Individuals who are unable to follow the introductions regarding the progress of trial for their medical, psychological, social, geographical conditions

研究者

相似试验

The efficacy of carnitine complex(The efficacy of... | 临床试验