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
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
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