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临床试验/NCT00832689
NCT00832689已完成2 期

Irinotecan, Gemcitabine, Chemotherapy for Biliary Tract Cancer

Yonsei University1 个研究点 分布在 1 个国家目标入组 39 人开始时间: 2008年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
39
试验地点
1

研究概览

简要总结

The study hypothesis is that chemotherapy of irinotecan and gemcitabine will improve local control of cancer and prolong survival in patients with inoperable biliary tract cancer.

研究设计

研究类型
Interventional
主要目的
Treatment

入排标准

年龄范围
17 Years 至 75 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically or cytologically confirmed inoperable biliary tract cancer
  • Age: 18 ~75 years old
  • Performance status: ECOG 0-2
  • Hematopoietic:
  • Granulocyte count at least 1,500/mm3
  • Platelet count at least 100,000/mm3
  • Bilirubin No greater than 2 fold the upper normal limit
  • AST/ALT : No greater than 3 fold the upper normal limit
  • Creatinine - no greater than 1.5 mg/dL
  • Not pregnant
  • No other serious medical or psychiatric illness that would preclude giving informed consent or limit
  • No prior chemotherapy within 6 months
  • No other concurrent anticancer radiotherapy within 6 months

排除标准

  • 未提供

研究组 & 干预措施

1

Experimental

干预措施: Irinotecan and Gemcitabine (Drug)

研究者

申办方类型
Other

研究点 (1)

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