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
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