ISRCTN07772084已完成未知
German Acute Hepatitis B Study: a double-blind placebo-controlled randomised two-armed parallel-group phase IIb multi-centre trial
niversity of Leipzig (Germany)0 个研究点目标入组 35 人开始时间: 2007年2月22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
- 35
研究概览
简要总结
2014 results in: https://www.ncbi.nlm.nih.gov/pubmed/24329913 (added 09/05/2019)
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. Acute hepatitis
- •2. HBsAg positive
- •3. Compensated liver function (Quick > 50%)
- •4. Bilirubin > 5mg/dl (i.e. >85µmol/l)
- •5. ALAT > 10 times upper normal range
- •6. Age >= 18 years
- •7. Hospitalization caused by acute hepatitis
- •8. Time since diagnosis < 8 days
- •9. Written informed consent of the patient
排除标准
- •1. Known or obvious pre-existing liver disease
- •2. Ongoing interferon therapy or stop of interferon less than 3 months ago
- •3. Ongoing drug abuse
- •4. HIV positive
- •5. Anti-HCV or HCV-RNA positive
- •6. Anti-HDV positive
- •7. Renal insufficiency (creatinine >1.5mg/dl or 135µmol/l)
- •8. Pregnant or nursing women
- •9. Women with child bearing potential (< 2 years after last menstruation) without effective contraception
- •10. Use of oral contraception
- •11. Patient with transplanted organs
- •12. Any disease requiring immunosuppressive therapy, incl. cancer chemotherapy
- •13. Any acute infectious disease requiring administration of sulphonamide/ trimethoprim
- •14. Evidence of any other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates use of an investigational drug, or patient at high risk from treatment complications
- •15. Known hypersensitivity to any of the study drugs or its ingredients
- •16. Current or recent (within 30 days prior to start of trial treatment) treatment with another investigational drug or participation in another investigational trial
- •17. Expected low compliance (e.g. by travel distance to trial site)
研究者
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