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临床试验/EUCTR2011-004201-25-NL
EUCTR2011-004201-25-NL进行中(未招募)不适用

The BOKITO-1B Study:Tenofovir DF Bone and Kidney Toxicity. Pharmacology in HBV monoinfected patients. - BOKITO-1B

Erasmus MC0 个研究点开始时间: 2011年10月5日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
Erasmus MC

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Inclusion criteria
  • Adult (> 18 years old), chronically HBV-infected, meeting the criteria for antiviral therapy
  • Group 1: 25 persons starting TDF with creatinine clearances between 50-80 mL/min
  • Group 2: 25 persons starting TDF with creatinine clearances of > 80 mL/min
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 50
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Exclusion criteria
  • Renal clearance (CG) < 50 mL/min, HIV- and/or HCV-co infection.

研究者

发起方
Erasmus MC

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