NCT02830867Unknown不适用
Review of French Cases of Glutathione Synthetase Deficiency
University Hospital, Strasbourg, France1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2016年7月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Immunologically determining human acid glutathione S-transferase in a human assay sample
研究概览
简要总结
The glutathione synthetase deficiency, inborn error of metabolism of autosomal recessive inheritance, is a rare disease (70 patients described in the world). The outcome of these patients and potential complications of this disease are not, to date, yet all known and described.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Immunologically determining human acid glutathione S-transferase in a human assay sample
时间窗: 1 hour after hospitalization
次要结局
未报告次要终点
研究者
研究点 (1)
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