跳至主要内容
临床试验/EUCTR2013-005475-41-BE
EUCTR2013-005475-41-BE进行中(未招募)不适用

Sulfamethoxazole treatment of primary PREPL deficiency - Sulfamethoxazole for HCS

Z Brussel0 个研究点开始时间: 2014年5月19日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

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

  • Diagnosis of hypotonia cystinuria syndrome or isolated PREPL deficiency by molecular genetics.
  • Able to be compliant with the study protocol.
  • Not of childbearing age (women).
  • Children and adults.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 15
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 8
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Not able to comply with the study protocol
  • Women of childbearing age
  • Concomitant neuromuscular disease

研究者

发起方
Z Brussel

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