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临床试验/NCT00443677
NCT00443677已完成3 期

Treatment of Advanced Hodgkin's Disease (Stages IIB-III-IV)

Gruppo Italiano Studio Linfomi1 个研究点 分布在 1 个国家目标入组 307 人开始时间: 2000年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
307
试验地点
1
主要终点
To compare the toxicity of the COPPEBVCAD vs BEACOPP vs ABVD regimens

研究概览

简要总结

The purpose of this study is to compare the toxicities of the COPPEBVCAD vs BEACOPP vs ABVD regimens.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically confirmed diagnosis of Hodgkin disease
  • Clinical stage IIB, III, IV
  • No prior treatment for Hodgkin disease or other malignancy
  • Age 18-65 year
  • Good cardiac, pulmunar, renal and hepatic function
  • Performance status 0-3 (Karnofsky 100- 40)
  • Written Informed Consent

排除标准

  • HIV positivity
  • Large cell, anaplastic, CD30+ lymphoma

研究组 & 干预措施

abvd

Active Comparator

干预措施: COPPEBVCAD vs BEACOPP vs ABVD (Drug)

beacopp

Experimental

干预措施: COPPEBVCAD vs BEACOPP vs ABVD (Drug)

coppebvcad

Experimental

干预措施: COPPEBVCAD vs BEACOPP vs ABVD (Drug)

结局指标

主要结局

To compare the toxicity of the COPPEBVCAD vs BEACOPP vs ABVD regimens

次要结局

  • To compare the results in terms of response, failure free survival and relapse free survival of the three regimens

研究者

发起方
Gruppo Italiano Studio Linfomi
申办方类型
Other

研究点 (1)

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