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临床试验/NCT04667299
NCT04667299Unknown4 期

Bismuth-Metronidazole Triple Versus Quadruple Therapy for Helicobacter Pylori First-line Treatment: A Randomized Controlled Trial

Shanghai Zhongshan Hospital1 个研究点 分布在 1 个国家目标入组 270 人开始时间: 2020年12月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
270
试验地点
1
主要终点
Eradication rate of Helicobacter pylori

研究概览

简要总结

This randomized controlled clinical trial will compare the eradication efficacy of bismuth-metronidazole triple therapy (PPI+bismuth+ metronidazole) with that of bismuth-metronidazole quadruple therapy (PPI+bismuth+ metronidazole+ amoxicillin) for Helicobacter pylori first-line treatment. The completion of this trial will expand new therapy for the treatment of Helicobacter pylori, which can not only ensure clinical efficacy, but also reduce the use of antibiotics.

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 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Participate in the trial voluntarily, fully understand the trial, and sign the informed consent form (ICF).
  • 18-75 years old on the day of signing the ICF.
  • Helicobacter pylori infection confirmed by 13C-urea breath test or rapid urease test.
  • Have not received Helicobacter pylori eradication treatment before.

排除标准

  • Have received Hp eradication treatment.
  • Patients with severe heart, lung, kidney, liver, blood, nerve, endocrine, and psychiatric diseases.
  • Subjects or guardians refused to participate in the trial.
  • Alcohol and/or drugs Abuse (addiction or dependence) or poor compliance with doctor's judgment.
  • Have taken antibiotics, bismuth, PPI or Chinese traditional medicine 4 weeks before treatment.
  • Pregnant or lactating women.
  • Active peptic ulcer.
  • allergic to drugs used in the trial.
  • any other circumstances that are not suitable for recruitment.

研究组 & 干预措施

BMT group

Experimental

Rabeprazole 20 mg bid, bismuth potassium citrate 0.6 g bid and metronidazole 0.4 g qid for 14 days

干预措施: Rabeprazole (Drug)

BMT group

Experimental

Rabeprazole 20 mg bid, bismuth potassium citrate 0.6 g bid and metronidazole 0.4 g qid for 14 days

干预措施: Bismuth potassium citrate (Drug)

BMT group

Experimental

Rabeprazole 20 mg bid, bismuth potassium citrate 0.6 g bid and metronidazole 0.4 g qid for 14 days

干预措施: Metronidazole (Drug)

BMQ group

Active Comparator

Rabeprazole 20 mg bid, bismuth potassium citrate 0.6 g bid, metronidazole 0.4 g qid and amoxicillin 1 g bid for 14 days

干预措施: Rabeprazole (Drug)

BMQ group

Active Comparator

Rabeprazole 20 mg bid, bismuth potassium citrate 0.6 g bid, metronidazole 0.4 g qid and amoxicillin 1 g bid for 14 days

干预措施: Bismuth potassium citrate (Drug)

BMQ group

Active Comparator

Rabeprazole 20 mg bid, bismuth potassium citrate 0.6 g bid, metronidazole 0.4 g qid and amoxicillin 1 g bid for 14 days

干预措施: Metronidazole (Drug)

BMQ group

Active Comparator

Rabeprazole 20 mg bid, bismuth potassium citrate 0.6 g bid, metronidazole 0.4 g qid and amoxicillin 1 g bid for 14 days

干预措施: Amoxicillin (Drug)

结局指标

主要结局

Eradication rate of Helicobacter pylori

时间窗: At least 4 weeks after completion of therapy

Eradication of Helicobacter pylori was defined as negative result of urea breath test (\<4‰ cut-off value).

次要结局

  • Eradication rate of Helicobacter pylori metronidazole-resistant strains(At least 4 weeks after completion of therapy)
  • Eradication rate of Helicobacter pylori metronidazole-susceptible strains(At least 4 weeks after completion of therapy)

研究者

发起方
Shanghai Zhongshan Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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