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临床试验/KCT0002450
KCT0002450招募中未知

Feasibility of quantitative measurement of several components in abdominal examination - for functional dyspepsia

Kyung Hee University Oriental Medicine Hospital at Gangdong0 个研究点目标入组 88 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
发起方
入组人数
88

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational Study

入排标准

年龄范围
20(Year) 至 65(Year)(—)
性别
All

入选标准

  • 1. Patient inclusion criteria
  • 1) Subjects between the ages of 20 and 65 years;
  • 2) Subjects who meet functional dyspepsia (FD) definition of Rome ? criteria;
  • 2-1) Subjects with one or more of these symptoms (such as postprandial fullness, early satiation, or epigastric pain or burning) will be considered patients with dyspepsia,
  • 2-2) and without organic disease basis that can explain symptoms,
  • 2-3) have undergone the above symptoms for a minimum of three months from at least six months ago to the present time.
  • 2. Control inclusion criteria
  • 1) Subjects who have no problem communication;
  • 2) Subjects who check less than 20 mm visual analogue scale for dyspeptic symptoms;
  • 3) Subjects who have not gastrointestinal disorder and symptoms;
  • 4) Subjects who have not serious structural diseases (disease of liver, heart, lung, or kidney);
  • 5) Subjects who have normal laboratory test result.

排除标准

  • 1) Subjects who have organic disease such as peptic ulcer or gastroesophageal reflux disease go through esophagogastroduodenoscopy and laboratory test;
  • 2) Subjects who have obvious signs of irritable bowel syndrome (IBS);
  • 3) Subjects who have alarm symptoms (e.g., weight loss, black or tar stool, or dysphagia);
  • 4) Subjects who have serious structural disease (e.g., disease of heart, lung, liver or kidney) or mental illness;
  • 5) Subjects who have had surgery related with the gastrointestinal tract, except for appendectomy more than six months ago;
  • 6) Subjects who are pregnant or breastfeeding;
  • 7) Subjects who have taken any other clinical trial within 1 months;
  • 8) Subjects who are human immunodeficiency virus (HIV) positive;
  • 9) Subjects who have difficulty in attending the trial (e.g., paralysis, severe mental or psychological abnormality, dementia, drug addiction, time constraint, severe disorder in vision or hearing, outpatient treatment impossibility, illiteracy).

研究者

发起方
Kyung Hee University Oriental Medicine Hospital at Gangdong

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