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临床试验/EUCTR2015-003539-37-Outside-EU/EEA
EUCTR2015-003539-37-Outside-EU/EEA进行中(未招募)不适用

An international, multicenter, randomized, open-label, parallel efficacy, and safety trial of intravenous zoledronic acid compared to intravenous pamidronate in children with severe osteogenesis imperfect.

ovartis0 个研究点目标入组 158 人开始时间: 2016年3月7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
ovartis
入组人数
158

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

  • Male or Female children between 3 months and 17 years old
  • OI type I, III or IV
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 158
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Deformity or abnormality which would prevent spine bone density from being done
  • Any surgical bone-lengthening procedure
  • Any kidney diseases or abnormalities
  • Low calcium or vitamin D levels in the blood
  • Other protocol-defined inclusion/exclusion criteria may apply.

研究者

发起方
ovartis

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