EUCTR2008-002299-92-IT进行中（未招募）不适用
METRONOMIC CAPECITABINE IN ADVANCED HEPATOCARCINOMA:A FASE II STUDY - Capemetro
AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI0 个研究点开始时间: 2008年7月8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）
- 发起方
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
- All
入选标准
- •Histologic proof of HCC or respect of Barcelona criteria
- •No possibility of curative treatments (surgery, RF, TACE or PEI)
- •Life expectancy > 3 months
- •Child-Pugh stage A or B
- •Total bilirubine < 3 mg/dl
- •Adequate bone marrow function
- •Adequate renal and cardiac function
- •Written informed consent
- •Child-Pugh A o B Bilirubina totale < 3 mg/dl
- •Adeguata riserva midollare
- •Adeguata funzionalita' renale e cardiaca
- •Consenso informato scritto
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •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
- •Severe cardiac or renal disease
- •Women of child-bearing potential that refuse adequate contraceptive measures, no
- •pregnancy or breast feeding
- •Child-Pugh stage C
- •History of hypersensitivity to 5-FU
- •Administration of any sperimental chemotherapeutic agents within the last two months
- •Any clinical conditions potentially hampering compliance with the study protocol
- •Any psychological, familial, social or geographical conditions potentially hampering
- •compliance with the study protocol
研究者
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