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临床试验/NL-OMON47599
NL-OMON47599招募中不适用

Characterization of platelets and antibodies in adult patients with immune thrombocytopenia (ITP) - Research into the development of ITP

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
30

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
18 至 64(—)

入选标准

  • Patients receiving corticosteroids, IVIG or TPO receptor agonists are allowed to participate. ;- Age minimal 18 years, both men and women
  • - Subjects with primary/chronic ITP (as defined by [Rodeghiero] with platelet numbers that have been below <30*10^9/L at one timepoint)
  • - Written informed consent
  • - WHO performance status <3

排除标准

  • - Prior treatment with rituximab as this will interfere with B-cell isolation
  • - Use of anticoagulants (e.g. NSAIDs) affecting platelet function
  • - Inadequate renal and liver function, i.e. creatinine or bilirubin >2.5 x the upper normal value
  • - Severe cardiac dysfunction
  • - Severe pulmonary dysfunction
  • - Severe neurological or psychiatric disease
  • - Any psychological, familial, sociological and geographical condition potentially hampering compliance with the study protocol
  • - Concurrent severe and/or uncontrolled medical condition (e.g. uncontrolled diabetes, hypertension, cancer, etc.)
  • - Neutrophil count <1.5*10^9/L and hemoglobin level <6.2 mmol/L.
  • - Active bleeding (defined by grade 3 or 4 according to NCI CTCAE v3.0)
  • - Pregnant or lactating
  • - Systemic infections: active viral infections, including HIV
  • - Seriously immunocompromised patients
  • - Systemic autoimmune disorders (e.g. systemic lupus erythematosus, SLE)
  • - Current malignant disease
  • - Any experimental therapy within 30 days prior to blood draw

研究者

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