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临床试验/NCT00770523
NCT00770523已完成不适用

Unrelated Donor Hematopoietic Stem Cell Transplantation After Nonmyeloablative Conditioning for Younger Patients With Hematologic Malignancies

Cooperative Study Group A for Hematology1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2003年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
52
试验地点
1
主要终点
treatment-related mortality and engraftment

研究概览

简要总结

Unrelated Donor Hematopoietic Stem Cell Transplantation After Nonmyeloablative Conditioning for Younger Patients with Hematologic Malignancies.

详细描述

Primary end points are treatment-related mortality and engraftment. Secondary end points are regimen-related toxicities, graft-versus-host-disease, relapse, and overall survival.

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
15 Years 至 55 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patients should have an unrelated donor who is matched for HLA-A and -B by serology and for -DRB1 by molecular typing.

排除标准

  • Patients should not have major illness or organ failure
  • Patients must not have a psychiatric disorder or mental deficiency severe as to make compliance with the treatment unlike, and making informed consent impossible.
  • Patients must not be pregnant or lactating.

结局指标

主要结局

treatment-related mortality and engraftment

时间窗: all cause mortality

次要结局

  • regimen-related toxicities, graft-versus-host-disease, relapse, and overall survival.(Time point(s) at which outcome measure is assessed.)

研究者

发起方
Cooperative Study Group A for Hematology
申办方类型
Network

研究点 (1)

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