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临床试验/NCT02412423
NCT02412423已完成4 期

Post-transplantation Cyclophosphamide for Haploidentical Transplant From Maternal or Collateral Donors

Peking University People's Hospital1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2015年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
30
试验地点
1
主要终点
rate of acute GVHD

研究概览

简要总结

In "beijing model" for haploidentical transplant, the rate of acute graft-versus-host disease (GVHD) from maternal or collateral donors was significantly higher than that from other kins. To reduce the GVHD incidence from maternal or collateral donors, post-transplantation cyclophosphamide is planned to be added into the protocol in "beijing model".

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • haploidentical patients from maternal or collateral donors

排除标准

  • uncontrolled infection before transplant

研究组 & 干预措施

treatment group

Experimental

post-transplantation cyclophosphamide

干预措施: post-transplantation cyclophosphamide (Drug)

结局指标

主要结局

rate of acute GVHD

时间窗: participants will be followed for an expected average of 365 days

次要结局

  • rate of relapse(participants will be followed for an expected average of 365 days)
  • rate of non-relapse mortality(participants will be followed for an expected average of 365 days)
  • probability of survival(participants will be followed for an expected average of 365 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Xiaojun Huang,MD

director

Peking University People's Hospital

研究点 (1)

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