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临床试验/NL-OMON23070
NL-OMON23070尚未招募不适用

Genotyping and phenotyping of skeletal deformities in patients with Osteogenesis Imperfecta

Isala, Zwolle0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • main inclusion criteria:
  • - Patients with confirmed Osteogenesis Imperfecta
  • - Adult (>18 years)
  • - Recent DEXA-scan ( < 3 years)

排除标准

  • main exclusion criteria:
  • - Patients who have had a fracture at recent medical history (<2 years) at both distal radii and tibiae.
  • - Patients who have had a malignancy at recent medical history (<2 years), who have been treated with glucocorticoids less than 3 months ago, who have severe kidney disease (eGFR <30 ml/min) or who suffer from other metabolic diseases affecting bone.
  • - Female patients who are pregnant.

研究者

发起方
Isala, Zwolle

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