跳至主要内容
临床试验/JPRN-UMIN000000884
JPRN-UMIN000000884已完成未知

A comparison of lamivudine plus adefovir and entecavir for chronic hepatitis B patients who had not previously received a nucleoside analogue: A randomized trial - LAM plus ADV vs ETV for nucleoside naive HBV patients, a randomized trial

niversity of Tokyo Department of Gastroenterology, Faculty of Medicine0 个研究点目标入组 200 人开始时间: 2007年11月13日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
200

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • The exclusion criteria are as follows: a previous history of a severe drug hypersensitivity against nucleoside analogues, malignancy within 5 years, severe renal disease (BUN more than 40 mg/dl or creatinine more than 2.0 mg/dl) the presence of other forms of liver disease such as auto immune hepatitis, coinfection with hepatitis C, history of liver transplantation, participation in another clinical trial, receiving prohibition medication for combination, and doctors' stop not to register to the study.

研究者

发起方
niversity of Tokyo Department of Gastroenterology, Faculty of Medicine

相似试验