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临床试验/NCT01380951
NCT01380951Unknown4 期

Clinical Study of Telbivudine on Liver Cirrhosis in Patients With Chronic Hepatitis B

The Fifth People's Hospital of Suzhou1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2011年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
120
试验地点
1
主要终点
Serum HBV DNA

研究概览

简要总结

Antiviral treatment on Chronic Hepatitis B (CHB) patients with liver cirrhosis is compulsory and effective. Telbivudine, which is superior to lamivudine in the treatment of CHB,is considered to be appropriate for the antiviral treatment on CHB patients with liver cirrhosis.

详细描述

Antiviral therapy on CHB patients with liver cirrhosis is compulsory and effective. Diseases development can be prevented or delayed if the virus is depressed successfully. Lamivudine is often used and usually has good efficacy. However, lamivudine resistance and virus mutation happens a lot. Telbivudine, which is superior to lamivudine in the treatment of CHB,is considered to be appropriate for the antiviral treatment on CHB patients with liver cirrhosis.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • liver cirrhosis with CHB
  • without history of antiviral therapy or discontinued antiviral therapy for more than 6 months
  • for patients with compensated liver cirrhosis: HBV DNA≥4log copies/ml if HBeAg positive,HBV DNA≥3log copies/ml if HBeAg negative
  • for patients with uncompensated liver cirrhosis:HBV DNA positive

排除标准

  • coinfection with HCV,HDV and HIV
  • AFP≥100mg/L or HCC diagnosed by iconography
  • with severe cardiovascular, respiratory and endocrinology diseases or autoimmune diseases

研究组 & 干预措施

telbivudine

Experimental

干预措施: telbivudine (Drug)

结局指标

主要结局

Serum HBV DNA

时间窗: 48 weeks

serum HBV DNA negativity and decline from baseline at week 48

次要结局

  • Serum HBeAg(48 weeks)
  • Child-pugh score(48 weeks)

研究者

发起方
The Fifth People's Hospital of Suzhou
申办方类型
Other

研究点 (1)

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