跳至主要内容
临床试验/KCT0004280
KCT0004280进行中(未招募)未知

The efficacy of hepatotonic drugs in several prescription patterns for the liver disease patients with elevated liver enzyme levels: a retrospective, comparative, phase ? study

Celltrion Pharm0 个研究点目标入组 906 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
进行中(未招募)
发起方
入组人数
906

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational Study

入排标准

年龄范围
19(Year) 至 o Limit(—)
性别
All

入选标准

  • 1. over 19 year old on the index date the first treated hepatotonic drugs
  • 2. Subjects who were treated hepatotonic drugs for over then 12 weeks and meet the following criteria
  • 1) Godex cap.: over then 168 cap/12 weeks
  • 2) Ursa tab.: over then 16,800 mg/12 weeks
  • 3) Legalon cap.: over then 168 cap/12 weeks
  • 4) Pennel cap.: over then 168 cap/12weeks
  • 3. outpatient
  • 4. Subjects who meet the hepatic function index (40 IU/L = ALT = 400 IU/L and AST = 400 IU/L)

排除标准

  • 1) Subjects with hepatic cirrhosis or malignancy
  • 2) Subjects with HBV, HCV(who weren’t treated anti-virus therapy, could be included)
  • 3) Subjects who administered hepatotonic drugs within 14 days of the index date
  • 4) Other subjects who are not eligible for this study

研究者

发起方
Celltrion Pharm

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