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临床试验/JPRN-UMIN000021790
JPRN-UMIN000021790未知未知

Efficacy and safety on effects of ribavirin with sofosbuir and ledipasvir combination therapy for patients who failed to daclatasvir and asunaprevir combination therapy - LDV/SOF+RBV combination therapy for patients with chronic hepatitis C who failed to DAC/ASV therapy

St. Marianna University School of Medicine0 个研究点目标入组 20 人开始时间: 2016年4月6日最近更新:
适应症

试验速览

阶段
未知
入组人数
20

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 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) HBV or HIV co-infected patients 2) Patients with a hepatocellular carcinoma, at the start of treatment 3) Patients with pregnancy, or possibility to be pregnant, or on breast feeding 4) Patients with a history of hypersensitivity to other nucleoside-analogue 5) Patients with severe renal dysfunction or need to be treated on hemodialysis 6) Patients with poorly controlled cardiac disease (e.g., myocardial infarction, cardiac failure, arrhythmia) 7) Patients with abnormal hemoglobin disease 8) Patients with severe depression, suicidal ideation, or severe mental illness 9) Patients with severe hepatic impairment 10) Patients with Autoimmune hepatitis 11) Patients taking medicine as below: rifampicin, phenytoin, carbamazepine, seiyouotogisou-including foods 12) Patients who took investigational agents within 3 months prior to this study 13) Patients who are unsuitable for study entry in the opinion of the principal investigator, for this study due to any other reason

研究者

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