跳至主要内容
临床试验/KCT0008756
KCT0008756尚未招募Unknown

Efficacy evaluation of digestive in patients who underwent gastrectomy for gastric cancer

ational Cancer Center0 个研究点目标入组 240 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
240

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
19(Year) 至 o Limit(—)
性别
All

入选标准

  • 1. Patients 19 years of age or older
  • 2. Patients who underwent gastrectomy for gastric cancer
  • 3. Patients who do not need adjuvant chemotherapy and under follow- up
  • 4. Patient having no abnormal finding in endoscopic examination at 3 months (±4 weeks), postoperatively
  • 5. Patients having postprandial satiety or early satiety for more than 3 days per week at 3 months (±4 weeks) after surgery (postprandial distress syndrome of ROMA IV classification, postprandial distress syndrome

排除标准

  • 1. Vulnerable subjects (pregnant patients, those lacking communication ability, etc.)
  • 2. Patients who have taken drugs classified as digestive agents within 7 days from the time of registration
  • 3. Patients taking drugs that affect digestive function an evaluation (anti-cancer drugs, adrenal cortical hormone drugs, anti-inflammatory drugs, etc.)
  • 4. Patients with genetic problems of galactose intolerance
  • 5. Patients judged unsuitable for participation in this study by the researcher

研究者

发起方
ational Cancer Center

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