NCT00822250已完成不适用
Clinical and Biological Study of Sub-pigmentation During Infantile Cystinosis
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 30
- 试验地点
- 2
- 主要终点
- to determine molecular mechanism of the disease
研究概览
简要总结
The purpose of this study is to determine the molecular mechanism of this disease and to research the relationship between cystinosis and skin phenotype.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 1 Year 至 15 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •known CTNS mutation
排除标准
- •patient with corticotherapy treatment
- •patient with immunosuppressant treatment
结局指标
主要结局
to determine molecular mechanism of the disease
时间窗: at time= 0
次要结局
- to research relationship between skin phenotype and cystinosis(at time =0)
研究者
研究点 (2)
Loading locations...
相似试验
已完成
不适用
Clinical and Genetic Studies of Familial Presenile Dementia With Neuronal Inclusion BodiesFamilial Dementia With Neuroserpin Inclusion BodiesNervous System Heredodegenerative DisorderNCT00006176National Human Genome Research Institute (NHGRI)100
终止
不适用
Analysis of Cutaneous and Hematologic Disorders by High-Throughput Nucleic Acid SequencingCutaneous LymphomaOther Skin DisordersMycosis FungoidesCutaneous T-cell LymphomaNCT01556828Stanford University70
招募中
不适用
Genetic Basis of Melanocytic NeviMelanocytic NeviNCT03054584University of California, Davis50
已完成
不适用
Function of the Pigment Epithelium in Patients With Type 1 NeurofibromatosisNeurofibromatosis Type 1NCT04153344Assistance Publique - Hôpitaux de Paris30
招募中
不适用
Genomic Study of Cutis TricolorDermatosis PigmentaryNCT06073171University Hospital, Montpellier10