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临床试验/NCT00725751
NCT00725751已完成不适用

Evaluation of Treatment of Chronic Hepatitis C With Pegylated Interferon and Ribavirin in Patients With/Without Substitution Therapy in Austria

Merck Sharp & Dohme LLC0 个研究点目标入组 353 人开始时间: 2007年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
353
主要终点
Number of Participants Who Completed Treatment With PegIFN-2b/Ribavirin

研究概览

简要总结

Although injection drug users represent the majority of new and existing cases of infection with hepatitis C virus (HCV), many lack access to treatment because of concerns about adherence, effectiveness, and reinfection. On the basis of a small but growing body of evidence showing that injection drug users can undergo treatment for HCV infection successfully, the 2002 NIH Consensus Statement on Hepatitis C has recommended that substance users be treated for HCV infection on a case-by-case basis. In this study, all patients will receive pegylated interferon alfa-2b (PegIFN-2b) and ribavirin according to European labeling; one cohort of participants will also be receiving substitution therapy (opioid medicines with long-lasting effects [methadone + buprenorphine] or morphine).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Adult patients with hepatitis C

排除标准

  • According to the products' European labeling

研究组 & 干预措施

PegIFN-2b/ribavirin with substitution therapy

Participants in this cohort received antiviral treatment and substitution therapy (opioid medicines with long-lasting effects [methadone + buprenorphine] or morphine)

干预措施: Pegylated interferon alfa-2b (PegIFN-2b) (Biological)

PegIFN-2b/ribavirin with substitution therapy

Participants in this cohort received antiviral treatment and substitution therapy (opioid medicines with long-lasting effects [methadone + buprenorphine] or morphine)

干预措施: Ribavirin (Drug)

PegIFN-2b/ribavirin without substitution therapy

Participants in this cohort received antiviral treatment but did not receive substitution therapy (opioid medicines with long-lasting effects [methadone + buprenorphine] or morphine)

干预措施: Pegylated interferon alfa-2b (PegIFN-2b) (Biological)

PegIFN-2b/ribavirin without substitution therapy

Participants in this cohort received antiviral treatment but did not receive substitution therapy (opioid medicines with long-lasting effects [methadone + buprenorphine] or morphine)

干预措施: Ribavirin (Drug)

结局指标

主要结局

Number of Participants Who Completed Treatment With PegIFN-2b/Ribavirin

时间窗: 24 to 48 weeks

For participants with Genotype 1 or 4 completion of treatment was at Week 48; for participants with Genotype 2, 3, or 1 with low viral load or rapid virologic response, completion of therapy was at Week 24.

次要结局

  • Number of Participants Who Achieved Sustained Virologic Response (SVR)(24 weeks after the end of treatment (i.e. 48 or 72 weeks depending on genotype))
  • Number of Participants Who Received Antiviral Treatment Who Were Also on Substitution Therapy(Day 1)

研究者

申办方类型
Industry
责任方
Sponsor

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