跳至主要内容
临床试验/KCT0004239
KCT0004239进行中(未招募)未知

Comparison of clinical outcomes after endoscopic submucosal dissection using high versus standard dose proton pump inhibitor : A prospective, randomized controlled trial

Kyung Hee University Hospital0 个研究点目标入组 438 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
进行中(未招募)
发起方
入组人数
438

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 o Limit(—)
性别
All

入选标准

  • 1)Over 19 years old patients who planned to undergo endoscopic submucosal dissection for gastric adenoma or early gastric caner.
  • 2) Person who are agreed upon study enrollement.

排除标准

  • 1)Coagulopathy defined by Prothrombine time > 1.5 INR, activated partial thromboplastin time > 1.5 times above reference value
  • 2)Previous history of stomach surgery
  • 3)Allergic to PPI (Hypersensitivity or history of hypersensitivity to PPI itself, constituent of PPI or Benzimidazole)
  • 4)Pregnant or lactating woman
  • 5)If it is impossible to assess one's pain
  • 6)Patients using atazanavir or nelfinavir
  • 7)Patients using Rilpivirine-containing medication

研究者

发起方
Kyung Hee University Hospital

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