跳至主要内容
临床试验/NCT02159976
NCT02159976已完成不适用

A Prospective, Multi-center, Randomized, Open-label, Parallel Design Clinical Trial to Compare 10-day Sequential Therapy and 14-day Modified Bismuth Quadruple Therapy for the Eradication of Helicobacter Pylori in Korea

Seoul National University Bundang Hospital1 个研究点 分布在 1 个国家目标入组 390 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
状态
已完成
入组人数
390
试验地点
1
主要终点
Counts of Participants With Successful H. Pylori Eradication

研究概览

简要总结

  1. To compare 10-day sequential therapy and 14-day modified bismuth quadruple therapy and to establish more effective first-line regimen for the eradication of Helicobacter pylori in Korea.
  2. To evaluate the effect of H. pylori eradication therapy on the symptom improvement of functional dyspepsia

详细描述

Emerging evidence shows that the eradication rate of proton pump inhibitor (PPI)-based triple therapy for the first-line treatment of Helicobacter pylori has decreased. The reason for the decrease in the efficacy of PPI-based triple therapy is mainly due to the increase in the resistance against clarithromycin. Sequential therapy seems to be more effective than the PPI-based triple therapy, however, the eradication rate of sequential therapy in Korea, which is mostly under 80%, is still not satisfactory. Modified bismuth quadruple therapy which replace metronidazole with amoxicillin (contained PPI, bismuth, tetracycline and amoxicillin) can be a promising regimen because the antibiotic resistance rate of tetracycline and amoxicillin are relatively low in Korea and amoxicillin is more easy to take in comparing with metronidazole. Therefore, the aim of this study is to compare 10-day sequential therapy and 14-day modified bismuth quadruple therapy and to establish more effective first-line regimen for the eradication of Helicobacter pylori in Korea.

In addition, previous studies reported that H. pylori infection also associated with functional dyspepsia (FD) and recommended H. pylori eradication in patients with FD. However, until now, there was no randomized prospective study in Korea, therefore the another aim of this study is to evaluate the effect of H. pylori eradication therapy on the symptom improvement of FD.

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
None

入排标准

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

入选标准

  • Male and female Korean Adult (Aged ≥ 18 years)
  • Patients who diagnosis of H. pylori infection by any of following three methods
  • positive rapid urease test (CLOtest)
  • histologic evidence of H. pylori by modified Giemsa staining
  • positive 13C-urea breath test

排除标准

  • Age under 18 years
  • Previous eradication treatment for H. pylori
  • Patients who took any drug which could influence the study results such as proton pump inhibitor, H2 blocker, mucosal protective agent and antibiotics
  • History of gastrectomy
  • Advanced gastric cancer or other malignancy
  • Abnormal liver function or liver cirrhosis
  • Abnormal renal function or chronic kidney disease
  • Other severe concurrent diseases
  • Previous allergic reactions to the study drugs
  • Pregnant or lactating women

研究组 & 干预措施

Sequential therapy

Active Comparator

pantoprazole 40mg bid 10 days (D1-D10), amoxicillin 1000mg bid 5 days (D1-D5), clarithromycin 500mg bid 5 days (D6-D10), metronidazole 500mg tid 5 days (D6-D10)

干预措施: Pantoprazole (Drug)

Sequential therapy

Active Comparator

pantoprazole 40mg bid 10 days (D1-D10), amoxicillin 1000mg bid 5 days (D1-D5), clarithromycin 500mg bid 5 days (D6-D10), metronidazole 500mg tid 5 days (D6-D10)

干预措施: Amoxicillin (Drug)

Sequential therapy

Active Comparator

pantoprazole 40mg bid 10 days (D1-D10), amoxicillin 1000mg bid 5 days (D1-D5), clarithromycin 500mg bid 5 days (D6-D10), metronidazole 500mg tid 5 days (D6-D10)

干预措施: Clarithromycin (Drug)

Sequential therapy

Active Comparator

pantoprazole 40mg bid 10 days (D1-D10), amoxicillin 1000mg bid 5 days (D1-D5), clarithromycin 500mg bid 5 days (D6-D10), metronidazole 500mg tid 5 days (D6-D10)

干预措施: Metronidazole (Drug)

Modified bismuth quadruple therapy

Experimental

pantoprazole 40mg bid 14 days (D1-D14) , amoxicillin 1000mg bid 14 days (D1-D14), tetracycline 1000mg bid 14 days (D1-D14), bismuth 600mg bid 14 days (D1-D14)

干预措施: Pantoprazole (Drug)

Modified bismuth quadruple therapy

Experimental

pantoprazole 40mg bid 14 days (D1-D14) , amoxicillin 1000mg bid 14 days (D1-D14), tetracycline 1000mg bid 14 days (D1-D14), bismuth 600mg bid 14 days (D1-D14)

干预措施: Amoxicillin (Drug)

Modified bismuth quadruple therapy

Experimental

pantoprazole 40mg bid 14 days (D1-D14) , amoxicillin 1000mg bid 14 days (D1-D14), tetracycline 1000mg bid 14 days (D1-D14), bismuth 600mg bid 14 days (D1-D14)

干预措施: Tetracycline (Drug)

Modified bismuth quadruple therapy

Experimental

pantoprazole 40mg bid 14 days (D1-D14) , amoxicillin 1000mg bid 14 days (D1-D14), tetracycline 1000mg bid 14 days (D1-D14), bismuth 600mg bid 14 days (D1-D14)

干预措施: Bismuth (Drug)

结局指标

主要结局

Counts of Participants With Successful H. Pylori Eradication

时间窗: 4 weeks after termination of eradication therapy, up to 6 weeks

次要结局

  • Functional Dyspepsia Symptom Responses Rate(1 year after termination of eradication therapy)
  • Counts of Participants Whose Drug Compliance is More Than 85%(4 weeks after termination of eradication therapy, up to 6 weeks)
  • Counts of Participants With Adverse Event(4 weeks after termination of eradication therapy, up to 6 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nayoung Kim

Professor, M.D, Ph.D.

Seoul National University Bundang Hospital

研究点 (1)

Loading locations...

相似试验

Compare Sequential and Quadruple Therapy for the... | 临床试验