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临床试验/NCT03348059
NCT03348059已完成不适用

Anti-E1E2 (D32.10 Epitope-binding) Antibodies Status Prior Therapy Favors Direct-acting Antiviral Treatment Efficacy

Hospices Civils de Lyon1 个研究点 分布在 1 个国家目标入组 103 人开始时间: 2015年10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
103
试验地点
1
主要终点
Proportion of patients with positive anti-E1E2 antibody level at treatment initiation

研究概览

简要总结

The hypothesis was to check whether baseline anti-E1E2 antibodies could predict virological outcome in Hepatitis C virus (HCV)-infected patients receiving direct-acting antiviral treatment

详细描述

Presence of anti-E1E2 antibodies was previously associated with spontaneous cure of hepatitis C virus (HCV). The hypothesis was to check whether baseline anti-E1E2 antibodies could predict virological outcome in HCV-infected patients receiving direct-acting antiviral treatment

研究设计

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

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
  • HCV patients treated with direct-acting antiviral treatment
  • Patients with a prior treatment blood sample
  • Patients with sustained virological response or virological relapse

排除标准

  • HIV or hepatitis B virus (HBV) coinfection

结局指标

主要结局

Proportion of patients with positive anti-E1E2 antibody level at treatment initiation

时间窗: Baseline (treatment initiation day)

Anti-E1E2 antibody levels were determined using optical densities obtained after dilution of patients' serum samples at 1/250 and 1/500. Samples with anti-E1E2 levels above 950 (OD value× 1000) were considered positive

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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