跳至主要内容
临床试验/NCT01057186
NCT01057186Unknown不适用

Hypophosphatemic Rickets in Norway

Haukeland University Hospital1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2009年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
80
试验地点
1
主要终点
Growth

研究概览

简要总结

The purpose of the study is to do a follow-up survey of all individuals with hereditary hypophosphatemia in Norway, focusing on manifestations in childhood and adolescence. The investigators also want to study phenotype-genotype associations, and look for new genes, in all forms of hereditary hypo and hyperphosphatemia.

研究设计

研究类型
Observational
观察模型
Cohort

入排标准

性别
All
接受健康志愿者

入选标准

  • All patients in the Norwegian population with hereditary hypophosphatemia, with or without rickets
  • Patients in the Norwegian population with hereditary hyperphosphatemia

排除标准

  • 未提供

研究组 & 干预措施

hereditary hypophosphatemia

Norwegian patients with hereditary hypophosphatemia.

干预措施: Alfacalcidol; phosphate. (Dietary Supplement)

Hereditary hyperphosphatemia

Norwegian patients with hereditary hyperphosphatemia (hyperphosphatemic familial tumoral calcinosis and hyperphosphatemia hyperostosis syndrome).

干预措施: Sevelamer (Drug)

结局指标

主要结局

Growth

时间窗: Up to 18 years

Change i height z-score from time of diagnosis to last registered consultation.

次要结局

未报告次要终点

研究者

发起方
Haukeland University Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Hypophosphatemic Rickets in Norway | 临床试验