EUCTR2013-000975-33-IS进行中（未招募）1 期
ovel Assays for the Determination of Urinary 2,8-Dihydroxyadenine and Other Key Urinary Purine Metabolites - Rare Diseases Clinical Research NetworkProtocol Version 1
andspitali - The National University Hospital of Iceland0 个研究点开始时间: 2013年10月3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）
- 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
- •Participants will be eligible for inclusion if they meet the following criteria:
- •1.Are patients 18 year and older who are enrolled in the APRT Deficiency Registry of The Rare Kidney Stone Consortium.
- •2.Control subjects who are either i) heterozygotes for an APRT mutation or ii) healthy individuals without mutation in the APRT gene.
- •3.Consent to participation in the study.
- •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 10
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 3
排除标准
- •1.Patients do not want to interrupt drug treatment as requested.
- •2.No other exclusion criteria if inclusion criteria are met.
研究者
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