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临床试验/EUCTR2018-001492-20-FI
EUCTR2018-001492-20-FI进行中(未招募)1 期

Pseudoxanthoma elasticum – supplementation therapy of pyrophosphate deficiency

Tampere university hospital0 个研究点目标入组 100 人开始时间: 2018年6月11日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
100

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

  • Adults (>18 yrs) are included when they have a clinically proven PXE. We will use the data from our earlier registry study to select patients with either mild to severe retinal changes or signs of an occlusive vascular disease.
  • 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 80
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 20

排除标准

  • Pregnancy, non-compliance or special groups according to researchers decision. Those without any signs of retinal or vascular disease are excluded. A fertile female without proper contraception.

研究者

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