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临床试验/ISRCTN61147621
ISRCTN61147621已完成不适用

CML IV - Chronic phase chronic myeloid leukaemia/CML 2000

Medical Research Council (MRC) (UK)0 个研究点目标入组 800 人开始时间: 2000年10月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
800

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

入选标准

  • 1. The interval from diagnosis to registration does not exceed 3 months (if received only hydroxyurea in these 3 months proceed to register, if alpha Interferon (IFN) has been given contact co-ordinators)
  • 2. They are aged 18-60; they have newly diagnosed CML
  • 3. They have acceptable criteria for chronic phase
  • 4. They have given informed consent and are willing to be randomised, there is no contraindication to collection of blood or marrow progenitor cells before treatment is commenced
  • 5. They are not pregnant

排除标准

  • Not provided at time of registration

研究者

发起方
Medical Research Council (MRC) (UK)

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