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临床试验/NCT02162316
NCT02162316Unknown不适用

A Multicenter, Randomized, Double-blind Comparative Study to Evaluate the Efficacy Between Helicobacter Pylori Eradication Therapy and Motilitone in Functional Dyspepsia

Chung-Ang University Hosptial, Chung-Ang University College of Medicine1 个研究点 分布在 1 个国家目标入组 136 人开始时间: 2014年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
136
试验地点
1
主要终点
Volunteer global assessment of improvement rate of functional dyspepsia by using 5-Likert scale

研究概览

简要总结

This is a clinical study to evaluate the efficacy between Helicobacter pylori Eradication therapy and Motilitone in Functional Dyspepsia

详细描述

This is a multicenter, randomized, double-blind comparative clinical study to evaluate the efficacy between Helicobacter pylori Eradication therapy and Motilitone in Functional Dyspepsia

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Roman III criteria
  • One or more conditions are applied: epigastric pain, epigastric burning, bothersome, postprandial fullness or early satiety
  • No organic lesion
  • Helicobacter pylori infection

排除标准

  • has taken prokinetics, H2 antagonists, PPIs, NSAIDs, anticholinergics, antibiotics, antidepressants, anticoagulants within a month
  • had a surgery that might affect gastrointestinal motility

研究组 & 干预措施

H.Pylori eradication therapy

Active Comparator

A-cillin®, Pantoline® and Clari® is administered with a tablet of placebo (Motilitone®)

干预措施: A-Cilin®, Clari® and Pantoline® (Drug)

Motilitone®

Experimental

30 mg is administered with 3 tablets of placebo (Patoline®, Clari® and A-cilin)

干预措施: Motilitone® (Drug)

结局指标

主要结局

Volunteer global assessment of improvement rate of functional dyspepsia by using 5-Likert scale

时间窗: 12 weeks

5-Likert scale 1. deteriorated 2. not changed 3. moderately improved 4. markedly improved 5. symptom-free

次要结局

  • Volunteer global assessment by using 5-Likert scale(6 weeks)
  • The improvement rate of 4 types of dyspepsia symptoms(12 weeks)
  • Assessment of NDI-K Quality of Life(6,12 weeks)
  • The change of each score and total score of dyspeptic symptoms(6, 12 weeks)
  • The proportion of the patients who answered "yes for the question about symptom improvement(6, 12 weeks)

研究者

发起方
Chung-Ang University Hosptial, Chung-Ang University College of Medicine
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jae Gyu Kim

Professor

Chung-Ang University Hosptial, Chung-Ang University College of Medicine

研究点 (1)

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