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临床试验/JPRN-UMIN000014777
JPRN-UMIN000014777尚未招募1 期

Study on safety and efficacy of granulocyte transfusion mobilized with G-CSF in related donor - Granulocyte transfusion from related donor

Kansai Medical University0 个研究点目标入组 10 人开始时间: 2014年8月13日最近更新:
适应症

试验速览

阶段
1 期
状态
尚未招募
入组人数
10

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 54years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • Recipient: not expected to survive more than 30 days, self hematopoiesis is not expected to recover within 30 days. Donor: allergy aginst G-CSF, pregnant or possible to be pregnant, breast feeding, history of thrombosisi or have risk of thrombosis, splenomegaly, comorbidiy or history of interstitial pneumonia, history of cancer, comorbidities of cardiac, pulmonary, renal diseases to be treated, comorbidities of inflammatory, autoimmune diseases to be treated.

研究者

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