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临床试验/KCT0004674
KCT0004674尚未招募未知

Effect of Aspirin for the Gastric Cancer Prevention in Early Gastric Cancer Patients Who Underwent Endoscopic Resection: a Randomized Controlled Trial

ational Cancer Center0 个研究点目标入组 1,700 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
1,700

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19(Year) 至 70(Year)(—)
性别
All

入选标准

  • 1. Men and women aged 19-70 who underwent endoscopic resection for early gastric cancer
  • 2. Final pathological results after endoscopic resection met the absolute or expanded criteria according to the Japanese Gastric Cancer Treatment guideline 2014 (version 4)
  • 3. Patients who had negative H. pylori status or those who eradicated H. pylori status
  • 4. Willingness to sign an informed consent form

排除标准

  • 1. Pateints who received aspirin for the secondary prevention of cardiovascular diseases or cerebrovascular diseases
  • 2. Regular aspirin uses (more than 3 times a week) with 2 months before screening visit
  • 3. Patients who used anticoagulants or antiplatelet drugs for therapeutic purpose
  • 4. Previous gastrectomy history
  • 5. Current treatment for serious medical condition which could hinder participation (such as severe heart dysfunction, liver cirrhosis, renal failure, COPD or bronchial asthma, or uncontrolled infection)
  • 6. High risk patients for bleeding complications (cerebral aneurysm, vascular malformation, esophageal or gastric varices, or hemophilia, etc)
  • 7. Active peptic ulcer disease (patients who treated peptic ulcer completely could be enrolled)
  • 8. Diagnosis and active treatment for other organ cancer (except carcinoma in situ, and non-melanoma skin cancer) within 5 years
  • 9. Non-curative resection of early gastric cancer after endoscopic resection
  • 10. Aspirin allergy or contraindication of aspirin use
  • 11. Pregnant or lactating women
  • 12. Alcoholism, drug abuse
  • 13. Inadequte patients for study enrollment according to the evaluation of the study physician
  • 14. Inability to provide an informed consent
  • 15. Patients who took a 28-day run-in-period medication less than 80%

研究者

发起方
ational Cancer Center

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