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临床试验/JPRN-UMIN000004352
JPRN-UMIN000004352招募中2 期

Phase II trial of Bevacizumab with XELOX as an adjuvant treatment after resection of colorectal liver metastases - Phase II trial of Bevacizumab with XELOX as an adjuvant treatment after resection of colorectal liver metastases (Miyagi-HBPCOG 007)

Tohoku University Graduate School of Medicine Division of Integrated Surgery and Oncology0 个研究点目标入组 45 人开始时间: 2010年10月10日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
45

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

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.Recurrence of chemotherapy of capecitabine, oxaliplatin and bevacizumab less than 6 months 2.Active multiple cancers (within 5 years) 3.Histry of hyper sensitivity against bevacizumab, oxaliplatin and capecitabine 4.Serious infections 5.Serious complications 6.Serious alteration or paresthesia interfering with function 7.Pregnancy woman, or woman with suspected pregnancy 8.Histry of organ recipient 9.Surgery, biopsy, specimen with section or sutures within the past 2 weeks. Fine needle aspiration biopsy within 1 week 10.Thrombosis with present or history of thromboembolism within the past 1 year 11.Administrated with Aspirin (>=325mg/day) or steroid for RA and chronic inflammatory disease 12.Untreatment of traumatic bone fracture 13.Require treatment of renal dysfunction, or urine protein >+2 within 2 weeks 14.Uncontrollable hypertension 15.Uncontrollable diarrhea 16.Uncontrollable peptic ulcer disease 17.Severe pulmonary disease (Interstitial pneumonitis or pulmonary fibrosis) 18.Cardiac disease (over grade2 by CTCAE v4.0).Or histry of myocardial infarction within 1 year 19.Doubting dihydropyrimidine dehydrogenase (DPD) deficit 20.Any subject judged by the investigator to be unfit for any reason to participate in the study

研究者

发起方
Tohoku University Graduate School of Medicine Division of Integrated Surgery and Oncology

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