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临床试验/JPRN-jRCT2080222040
JPRN-jRCT2080222040未知2 期

Phase II/III clinical trial of L-105 in patients with hepatic encephalopathy

ASKA Pharmaceutical Co., Ltd.0 个研究点目标入组 180 人开始时间: 2013年3月14日最近更新:
适应症

试验速览

阶段
2 期
入组人数
180

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
>= 20age old 至 <= 74age old(—)
性别
All

入选标准

  • Diagnosed as hepatic cirrhosis. In addition, patients having portal-systemic shunt without hepatic cirrhosis are eligible.
  • -Hyperammonemia
  • -Grade I or II mental state of H.E. (Classification by Inuyama Symposium)

排除标准

  • -A concurrent mental illness
  • -Acute hepatitis or in the acute exacerbation phase of chronic hepatitis
  • -Concurrent hepatocellular carcinoma. However, patients, who were locally treated with hepatectomy, radio-frequency ablation (RFA), transcatheter hepatic arterial embolization (TAE), or percutaneous ethanol injection therapy (PEIT) 4 weeks prior to the start of study medication, are eligible.
  • -Planning to receive new treatment for hepatocellular carcinoma during the study period
  • -Likely to undergo liver transplant within 6 months after enrollment

研究者

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