CTRI/2018/03/012644已完成2 期
A Randomized Clinical End Point Study To Evaluate The Safety And Efficacy Of CLEARLIV Tablets In Patients With Alcoholic Liver Disease. - ALD
Apex Laboratories0 个研究点目标入组 24 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 24
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
入选标准
- •1.Chronic alcohol intake patients
- •2.Serum AST &ALT is typically elevated to a level of 2â??6 times the upper limits of the normal.
- •3.Negative pregnancy test for women in reproductive age (up to two weeks prior to the study)
- •4.Negative for hepatitis B and C
排除标准
- •1.Patients who have liver disease with the cause different from that of alcohol induced liver disease.
- •2.Drug dependence
- •3.A known hypersensitivity or allergy to any component of the drugs evaluated in the study.
研究者
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