跳至主要内容
临床试验/EUCTR2007-006645-41-NL
EUCTR2007-006645-41-NL进行中(未招募)不适用

The (cost)effectiveness of paricalcitol in the treatment of secondary hyperparathyroidism in hemodialysis patients. - CEPS

Sint Lucas Andreas Hospital0 个研究点开始时间: 2008年5月29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

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

  • - Hemodialysis patients of 18 years and older.
  • - Secondary hyperparathyroidism.
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Severe hypercalcemia (Ca2+ > 2,65 mmol/L)
  • Severe hepatic dysfunction
  • Overdosage of digoxin
  • Hypersensitivity to vitamin D or overdosage of vitmain D
  • Parathyroidectomia in the past
  • < 18 years of age
  • Mentall illness

研究者

发起方
Sint Lucas Andreas Hospital

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