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临床试验/EUCTR2006-005728-17-IT
EUCTR2006-005728-17-IT进行中(未招募)不适用

Hormone-refractory Prostate cancer first Line Intermittent Taxotere and Estramustine. - ND

AZIENDA PROVINCIALE PER I SERVIZI SANITARI DELLA PROVINCIA AUTONOMA DI TRENTO0 个研究点目标入组 128 人开始时间: 2007年1月16日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
128

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Male

入选标准

  • 1 histologically proven diagnosis of prostate cancer 2 previous therapy with LHRH-analogue 3 PSA value rise during second line hormonal manipulation 4 performance status less than ECOG 2 5 life expectancy more than 12 weeks 6 adequate bone marrow function 7 written consent informed 8 patients ability to fill the quality of life questionnaire
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1 disease progression without PSA rise 2 active infection 3 previous chemotherapy for prostate cancer 4 non adequate liver or renal functions 5 major diseases limiting chemotherapy 6 major cardiovascular diseases

研究者

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