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临床试验/NCT00838019
NCT00838019Unknown4 期

Pilot Study About Viability and Efficacy of Intrabone Administration of Umbilical Cord Blood for Allogeneic Stem Cell Transplantation

Hospital Clinic of Barcelona2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2009年2月最近更新:
适应症

试验速览

阶段
4 期
入组人数
10
试验地点
2
主要终点
Kinetics of hematopoietic engraftment

研究概览

简要总结

The purpose of this study is to evaluate the viability of intrabone administration of umbilical cord blood as allogenic transplantation for the treatment of hematologic malignancies.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Hematological malignancies
  • Indication of allogenic transplantation
  • No suitable donor (related/unrelated)
  • No suitable cord blood unit with enough cellularity for standard transplant
  • Written informed consent

排除标准

  • ECOG > 2
  • Co-morbidities
  • HIV positive serology
  • Pregnancy or breastfeeding
  • Psychiatric illness

结局指标

主要结局

Kinetics of hematopoietic engraftment

时间窗: days 14, 21, 28 after administration

次要结局

  • Dynamics and chimerism of hematological engraftment(days 14, 21, 28 after administration)

研究者

申办方类型
Other

研究点 (2)

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