跳至主要内容
临床试验/NCT03346941
NCT03346941已完成不适用

Side Effects After Direct-acting Antiviral Treatment in Patients With Chronic Hepatitis C. The EFINO-C Study.

Hospices Civils de Lyon1 个研究点 分布在 1 个国家目标入组 95 人开始时间: 2016年5月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
95
试验地点
1
主要终点
Incidence of side effects

研究概览

简要总结

The objective of this study was to assess the incidence of side effects after direct-acting antiviral therapy in patients with chronic hepatitis C virus infection.

详细描述

Direct-acting antiviral (DAA)-based treatments are today very effective The objective of this study was to assess the incidence of side effects after DAA therapy in patients with chronic hepatitis C virus infection.

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

  • 18 years of age or older
  • Hepatitis C virus infection
  • Treatment by direct-acting antiviral combination

排除标准

  • HIV coinfection

结局指标

主要结局

Incidence of side effects

时间窗: Within treatment duration, i.e. 8, 12 or 24 weeks after treatment initiation

Incidence of side effects occurring during treatment duration. Treatment duration may be of 8 weeks, 12 weeks or 24 weeks depending on treatment combination.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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