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临床试验/ACTRN12615001063505
ACTRN12615001063505招募中未知

Determinants of sustained virological response after discontinuation of long-term nucleoside analogue therapy in chronic hepatitis B patients.

Professor Alexander Thompson0 个研究点目标入组 200 人开始时间: 2015年10月12日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
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
分配方式
Non-randomised trial
主要目的
Treatment

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Male or Female, age >18 years
  • Subjects must be able to understand and agree to comply with the prescribed intervention (NA cessation), visits and reliably communicate with study personal about adverse events
  • Able to provide informed consent.
  • Chronic Hepatitis B virus infection
  • HBeAg negative at time if initiation of NA therapy
  • Meet current APASL guidelines for consideration of antiviral cessation:
  • - uninterrupted NA treatment for >2 years and
  • - undetectable serum HBV DNA on three separate occasions >= 6 months apart (undetectable defined by a value < lower limit of detection using a sensitive commercial PCR assay)
  • Normal serum ALT levels (according to the uppers limit of normal of the local laboratory)
  • Minimal to moderate liver fibrosis defined as:
  • - METAVIR liver fibrosis stage F0-F3 inclusive prior to initial NA therapy and/or
  • - Transient liver elastogram (TLE) (Fibroscan) < /= 9.6 kPa at screening

排除标准

  • HBeAg positive chronic hepatitis B at the time of NA initiation
  • HBV associated extra hepatic manifestations
  • Documented or suspected hepatocellular carcinoma (HCC)
  • History of decompensated liver disease
  • Compensated cirrhosis defined as:
  • - METAVIR liver fibrosis stage 4 on pre-treatment biopsy; OR
  • - TLE > 9.6 kPa at screening
  • Co-infection with HIV,HCV or HDV
  • Latrogenic or disease related immunosuppression (e.g. treatment with systemic glucocorticoids, TNFa-antibodies, and other immunosuppressive drugs)
  • Significant alcohol consumption (> 30 g/day for women and > 50 g/day for men)
  • Current known history of cancer within 5 years of screening
  • Pregnant or breast feeding
  • Other known significant liver disease (including but not limited to haemochromatosis, autoimmune hepatitis, alcoholic liver disease)
  • Participation in any other interventional trial
  • Poor Venous access
  • Suspected lack of compliance
  • Any medical or social reason which in the opinion of the investigator would make the subject inappropriate for the study

研究者

发起方
Professor Alexander Thompson

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