Efficacy And Safety of Bismuth-Tetracycline-Rabeprazole Triple For First-Line Eradication of Helicobacter Pylori Infection
Efficacy And Safety of Bismuth-Tetracycline-Rabeprazole Triple Versus Bismuth Quadruple Therapies For First-Line Eradication of Helicobacter Pylori Infection: A Single-Center, Randomized Controlled Trial
研究概览
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Chih-An Shih, Doctor of Medicine
- 电话号码:886-8-8329966
- 邮箱:dreric921@gmail.com
研究联系人备份
- 姓名:Chang-Yi Li, Bachelor
- 电话号码:886-8-8329966
- 邮箱:victorlee0702@hotmail.com
学习地点
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Pingtung City、台湾、928004
- Antai Medical Care Corporation, Antai Tian-Sheng Memorial Hospital
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
adult patients (aged ≥18 years) who underwent esophagogastroduodenoscopy for the evaluation of gastrointestinal symptoms at Antai Tian-Sheng Memorial Hospital. Eligible individuals were invited to participate in an H. pylori screening program. Those who met either of the following criteria were considered for enrollment: (1) positive results from both the rapid urease test and histology, or (2) a positive culture result.
Exclusion Criteria:
(1) previous H. pylori eradication therapy, (2) a history of gastrectomy, (3) allergy to any of the eradication medications used in this study, (4) antibiotic use within 4 weeks before treatment, (5) the absence of post-treatment assessment for H. pylori eradication.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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有源比较器:Bismuth-Tetracycline-Rabeprazole Triple Therapy
Bismuth、Tetracycline、Rabeprazole
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14-day Bismuth-Tetracycline-Rabeprazole Triple
其他名称:
Bismuth quadruple therapy, combining Rabeprazole, Tetracycline, Bismuth, and Metronidazole
其他名称:
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有源比较器:Bismuth Quadruple Therapy
Bismuth、Tetracycline、Rabeprazol、Metronidazole
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14-day Bismuth-Tetracycline-Rabeprazole Triple
其他名称:
Bismuth quadruple therapy, combining Rabeprazole, Tetracycline, Bismuth, and Metronidazole
其他名称:
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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eradication rate
大体时间:6 weeks
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Follow-up at week 2 will assess treatment adherence and adverse events.
H. pylori status will be evaluated at week 6 using the C13-urea breath test.
Eradication and adverse event rates will be compared between groups using the chi-square test.
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6 weeks
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合作者和调查者
调查人员
- 首席研究员:Chih-An Shih, Doctor of Medicine、Antai Medical Care Corporation, Antai Tian-Sheng Memorial Hospital
出版物和有用的链接
一般刊物
- Gao W, Liu J, Wang X, Li J, Zhang X, Ye H, Li J, Dong X, Liu B, Wang C, Xu Y, Teng G, Tian Y, Dong J, Ge C, Cheng H. Simplified Helicobacter pylori therapy for patients with penicillin allergy: a randomised controlled trial of vonoprazan-tetracycline dual therapy. Gut. 2024 Aug 8;73(9):1414-1420. doi: 10.1136/gutjnl-2024-332640.
- Gao W, Xu Y, Liu J, Wang X, Dong X, Teng G, Liu B, Dong J, Ge C, Ye H, Zhang X, Cheng H. A real-world exploratory study on the feasibility of vonoprazan and tetracycline dual therapy for the treatment of Helicobacter pylori infection in special populations with penicillin allergy or failed in previous amoxicillin-containing therapies. Helicobacter. 2023 Apr;28(2):e12947. doi: 10.1111/hel.12947. Epub 2023 Jan 17.
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- AntaiMedCare
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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