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临床试验/NCT00569842
NCT00569842已完成不适用

Investigation of the Cylex® ImmuKnow® Assay

Indiana University School of Medicine1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2007年11月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
45
试验地点
1

研究概览

简要总结

Currently, there is no accurate way of predicting the occurrence of Graft vs Host Disease (GvHD) or infection. The purpose of this study is to analyze blood with the ImmuKnow® Assay to see if doctors can detect which patients are at risk for GvHD and for getting an infection before they occur.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who are undergoing allogeneic HSCT using a myeloablative preparative regimen for any of the following disorders are eligible:
  • Acute leukemia
  • Non-Hodgkin's Lymphoma
  • Chronic lymphocytic leukemia
  • Hodgkin's disease
  • Multiple myeloma
  • Myelodysplastic Syndromes
  • Myeloproliferative Disorders
  • Aplastic Anemia
  • Chronic myelogenous leukemia

排除标准

  • 未提供

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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