跳至主要内容
临床试验/JPRN-UMIN000053630
JPRN-UMIN000053630尚未招募Unknown

A Prospective Interventional Trial of Combination Therapy with hepatic arterial infusion of 5-FU and systemic infusion of Gemcitabine as Postoperative Adjuvant Therapy for Pancreatic Cancer - A Prospective Interventional Trial of Combination Therapy with hepatic arterial infusion of 5-FU and systemic infusion of Gemcitabine as Postoperative Adjuvant Therapy for Pancreatic Cancer

niversity of Toyama0 个研究点目标入组 75 人开始时间: 2024年2月16日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
75

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) Active multiple carcinoma (synchronous multiple carcinoma and heterochronic multiple carcinoma with a disease-free interval of 5 years or less) However, active multiple carcinoma does not include intraepithelial carcinoma or intramucosal carcinoma equivalent lesions that are considered curable with local treatment. 2) Have clear infection or inflammation requiring systemic treatment. 3) Fever of 38.0 degrees or higher at the time of enrollment 4) Allergy or contraindication to 5-FU or gemcitabine 5) History of serious drug hypersensitivity or drug allergy 6) Allergy to contrast media that precludes contrast studies 7) Serious cardiac disease or history of cardiac disease 8) Serious underlying disease (uncontrolled diabetes mellitus, renal failure, cirrhosis, etc.) 9) Has ascites or pleural effusion that is difficult to control 10) Active gastrointestinal bleeding requiring repeated blood transfusions 11) Diarrhea (more than 4 times a day or watery stools) 12) Uncontrolled cancer pain 13) Pulmonary fibrosis or interstitial pneumonia evident on imaging or clinical findings 14) Pregnant or lactating woman or possible (intended) pregnancy 15) Psychiatric illness or psychiatric symptoms that would preclude participation in the study 16) Unable to give consent to participate in this study

研究者

发起方
niversity of Toyama

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