DRKS00011383招募中不适用
Autoimmune-Lymphproliferative Primary Immunodeficiencies: A clinical, immunological and genetic cohort study (AL-PID study, formerly: ALPS study) - AL-PID (formerly: ALPS)
niversitätsklinikum FreiburgCentrum für Chronische Immundefizienz (CCI)0 个研究点目标入组 600 人开始时间: 2016年12月21日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 600
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 1 Years 至 18 Years（—）
- 性别
- All
入选标准
- •1.Chronic benign lymphoproliferation (i.e. splenomegaly +/- lymphadenopathy at 2 sites without infectious or malignant cause)
- •2.Autoimmune disease (i.e. AI cytopenia OR inflammatory bowel disease OR CNS inflammatory disease OR interstitial lung disease)
- •one of the two above manifestions
- •3.At least one factor indicating a primary immunodeficiency (i.e. infection susceptibility OR additional autoimmune or inflammatory manifestations OR hypogammaglobulinemia OR aberrant immunophenotype OR positive family history OR consanguinity)
排除标准
- •No written informed consent of patient or parents (in case of minors) has been obtained
研究者
相似试验
招募中
不适用
'Smoldering' autoimmune inflammatory pathophysiology in epilepsiesEpilepsyJPRN-UMIN000006800Kyoto University School of Medicine50
招募中
不适用
Pathophysiological study for autoimmune dysregulation of hereditary angioedemaHereditary angioedemaJPRN-UMIN000010754Juntendo Hospital50
招募中
不适用
To elucidate pathology of autoimmune disease and develop new treatmentautoimmune diseasesJPRN-UMIN000017559Keio University200
招募中
不适用
Autoimmune inflammation as cause of RelapsIng Symptoms in patients with viral EncephalitisViral encephalitisautoimmune encephalitisNL-OMON55224Academisch Medisch Centrum25
招募中
不适用
Immune-mediated polyneuropathy/chronic inflammatory demyelinating polyneuropathy (CIDP): diagnostic, prognostic, and treatment-response markersG61Inflammatory polyneuropathyDRKS00032455Charité - Universitätsmedizin Berlin320