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
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