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临床试验/NCT02553083
NCT02553083Unknown4 期

High Dose Dual Therapy (HDDT) for Eradication of Helicobacter Pylori Infection

Rabin Medical Center1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2015年10月22日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
300
试验地点
1
主要终点
Eradication rate

研究概览

简要总结

The investigators will performed a large-scale multi center trial to compare the efficacy of a high-dose dual therapy (HDDT) with that of standard therapies in treatment-naive (n = 300) patients with Hp infection. Consecutive symptomatic patients will be recruited in Israel and Spain when tested positive to Hp with serology and 13C urea breath test (13C-UBT) due to symptoms. Patients with gastric cancer, MALT lymphoma, and younger than 18 or older than 80 years old will be excluded. All patients will be naive to eradication therapy and will be randomized into one of three groups:

Group 1: Nexium 40 mg and amoxicillin 1.5 gr twice daily for 14 days Group 2: Nexium 40 mg and doxycycline 200 mg twice a day Group 3: Triple therapy of Nexium 20 mg, clarythromycin 500 mg, and amoxicillin 1gr twice a day for 10 days (regular accepted treatment).

All treatments will be stopped for a month and then 13CUBT will be repeated. The primary aim of the study is to assess eradication success, intentioned to treat and per protocol in the three treatment regimens.

The secondary aim of the study is to assess the safety of high dose amoxicillin and doxycycline.

详细描述

Introduction High dose dual therapy (HDDT) for Helicobacter pylori (Hp) eradication was successfully tried in Taiwan for naive as well as experienced patients who failed a previous trial. This new approach relies on the rare resistance of Hp to amoxicillin which is about 1% all over the world. High intra gastric pH increases the efficacy of amoxicillin, thus the "old" dual therapy with a proton pump inhibitor and amoxicillin, but now in high doses for a longer time, has a potential to achieve a high eradication rate. Yang and co investigators randomized 450 naïve and 168 treatment-experienced patients in Taiwan, all infected by Hp, for HDDT, sequential and triple therapies. In the intention-to-treat analysis, Hp was eradicated in 95.3%, 85.3% and 80.7%, respectively in naïve, and 89.3%, 51.8% and 78.6%, respectively in experienced patients. No more adverse events were found in the HDDT group. They divided the high dose of amoxicillin into 4 doses a day. This approach may be unnecessary since Kim and colleagues demonstrated the same results when the same dose of amoxicillin was divided into 2 or 4 times a day. Recently doxcycylin was found effective in triple or quadruple therapy regimens with no adverse effect in the high dose of 200 mg BID.

The investigators will try that approach, successful in Asian patients, in a collaborative study that included Spanish and Israeli patients. The investigators will investigate whether a combination of a high-dose proton pump inhibitor and amoxicillin (dual therapy) will be more effective than standard first-line 10 days triple therapy in eradicating Hp. Since patients who are allergic to penicillin cannot be treated with amoxicillin The investigators will compare HDDT amoxicillin-based therapy also with HDDT doxycycline -based therapy.

Protocol

The investigators will performed a large-scale multi center trial to compare the efficacy of a high-dose dual therapy (HDDT) with that of standard therapies in treatment-naive (n = 300) patients with Hp infection. Consecutive symptomatic patients will be recruited in Israel and Spain when tested positive to Hp with serology and 13CUBT due to symptoms. Patients with gastric cancer, MALT lymphoma, and younger than 18 or older than 80 years old will be excluded. All patients will be naive to eradication therapy and will be randomized into one of three groups:

Group 1: Nexium 40 mg and amoxicillin 1.5 gr twice daily for 14 days Group 2: Nexium 40 mg and doxycycline 200 mg twice a day Group 3: Triple therapy of Nexium 20 mg, clarythromycin 500 mg, and amoxicillin 1gr twice a day for 10 days (regular accepted treatment).

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

入选标准

  • Patients infected with Helicobacter pylori

排除标准

  • Patients with gastric cancer or MALT lymphoma

研究组 & 干预措施

Group 1

Active Comparator

Nexium 40 mg and amoxicillin 1.5 gr twice daily for 14 days

干预措施: Nexium 40 mg (Drug)

Group 1

Active Comparator

Nexium 40 mg and amoxicillin 1.5 gr twice daily for 14 days

干预措施: amoxicillin 1.5 gr (Drug)

Group 2

Active Comparator

Nexium 40 mg and doxycycline 200 mg twice daily for 14 days

干预措施: Nexium 40 mg (Drug)

Group 2

Active Comparator

Nexium 40 mg and doxycycline 200 mg twice daily for 14 days

干预措施: doxycycline 200 mg (Drug)

Group 3

Active Comparator

Nexium 20 mg, clarythromicin 500 mg, and amoxicillin 1 gr twice daily for 14 days

干预措施: Nexium 20 mg (Drug)

Group 3

Active Comparator

Nexium 20 mg, clarythromicin 500 mg, and amoxicillin 1 gr twice daily for 14 days

干预措施: clarythromicin 500 mg (Drug)

Group 3

Active Comparator

Nexium 20 mg, clarythromicin 500 mg, and amoxicillin 1 gr twice daily for 14 days

干预措施: amoxicillin 1gr (Drug)

结局指标

主要结局

Eradication rate

时间窗: 2 weeks therapy

Eradication rate

次要结局

未报告次要终点

研究者

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

Yaron Niv

Chief of Gastroenterology, Deputy CEO RMC

Rabin Medical Center

研究点 (1)

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