JPRN-UMIN000025085招募中未知
Efficacy and safety of ombitasvir/paritaprevir/ritonavir, ledipasvir/sofosbuvir, elbasvir /grazoprevir, glecaprevir/pibrentasvir after curative treatment of HCV-Related HCC - Prospective multicenter-cooperative cohort study - Ombitasvir/paritaprevir/ritonavir, ledipasvir/sofosbuvir, elbasvir/grazoprevir, glecaprevir/pibrentasvir therapy in HCV-Related HCC patients - Prospective multicenter-cooperative cohort study
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 90years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1)Patients who have a history of hypersensitivity to Omvitasvir/paritaprevir/ritonavir 2)Patients who are excluded from HCV eradication therapy because of decompensated cirrhosis and others 3)Patients who cannot receive IFN-free therapy because of concomitant medication etc. 4)Women who are or may be pregnant 5)Patients considered to be ineligible for participation in the study by the investigator or subinvestigators
研究者
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