NL-OMON39260已完成不适用
Effect of Telaprevir in triple therapy for chronic hepatitis C patients on Intrahepatic immunological Mechanisms - ETIM
Stichting Maag-, Darm- en Leveronderzoek0 个研究点目标入组 25 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 25
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •Patients between 18 and 70 years of age, with a chronic hepatitis C - genotype 1 infection.
- •Patients are naive, non-responders or relapsers to previous treatment with peginterferon or conventional interferon plus ribavirin combination therapy.
- •High viral load (>400,000 IU/ml)
- •Indication for antiviral therapy of hepatitis C according to current clinical guidelines.
- •Written informed consent.
排除标准
- •Signs of progressive liver disease, beyond generally accepted criteria for HCV antiviral therapy
- •History or other evidence of severe illness, malignancy or any other condition which would make the patient, in the opinion of the investigators, unsuitable for the study
- •Co-infections with human immunodeficiency virus (HIV) or Hepatitis B virus (HBV).
- •Presence of contra-indications for antiviral therapy with telaprevir, peginterferon or ribavirin.
- •Interfering substance abuse, such as alcohol (indicator: 28 drinks/ week).
- •Earlier treatment with a protease/polymerase inhibitor or treatment with peginterferon/ ribavirin within 6 months before start of therapy
- •Any other condition which in the opinion of the investigator would make the patient unsuitable for enrollment, or could interfere with the patient participating and completing in the study.
研究者
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