Feedback

Efficacy and safety of high-dose ilaprazole-amoxicillin dual therapy for Helicobacter pylori eradication: a prospective, single-center, randomized trial

Affiliation
Department of Gastroenterology and Oncology ,Civil Aviation General Hospital ,Beijing ,China
Cheng, Jianping;
Affiliation
Department of Gastroenterology and Oncology ,Civil Aviation General Hospital ,Beijing ,China
Fan, Chanjuan;
Affiliation
Department of Gastroenterology and Oncology ,Civil Aviation General Hospital ,Beijing ,China
Huang, Kun;
Affiliation
Department of Gastroenterology and Oncology ,Civil Aviation General Hospital ,Beijing ,China
Zhai, Lili;
Affiliation
Department of Gastroenterology and Oncology ,Civil Aviation General Hospital ,Beijing ,China
Wang, Hui;
Affiliation
Department of Gastroenterology and Oncology ,Civil Aviation General Hospital ,Beijing ,China
Xie, Dongling;
Affiliation
Department of Gastroenterology and Oncology ,Civil Aviation General Hospital ,Beijing ,China
Cai, Yong;
Affiliation
Department of Gastroenterology and Oncology ,Civil Aviation General Hospital ,Beijing ,China
Li, Zhen;
Affiliation
Department of Gastroenterology and Oncology ,Civil Aviation General Hospital ,Beijing ,China
Bai, Qixuan;
Affiliation
Department of Gastroenterology and Oncology ,Civil Aviation General Hospital ,Beijing ,China
Wang, Pan;
Affiliation
Department of Gastroenterology and Oncology ,Civil Aviation General Hospital ,Beijing ,China
Ding, Haiou

Background: Until now, there have been no randomized controlled trials directly evaluating the efficacy of high-dose ilaprazole-amoxicillin dual therapy (HT) in comparison to other standard treatments for H. pylori ( Helicobacter pylori ) infection. This study aimed to compare the effectiveness and safety of HT with bismuth quadruple therapy (BQT) as an initial treatment for H. pylori . Methods: This single-center, prospective, randomized clinical controlled trial recruited 225 consecutive patients. They were assigned to either HT group (ilaprazole, 10 mg, twice daily; amoxicillin 1,000 mg, three times daily) or BQT group (compound bismuth aluminate granules, 2.6 g, three times daily; ilaprazole, 5 mg, twice daily; amoxicillin, 1,000 mg, twice daily; clarithromycin, 500 mg, twice daily) for 14 days. The 13 C-urea breath test assessed eradication success 4 weeks after treatment. The primary outcome focused on the eradication rate, with secondary outcomes including safety and compliance. Results: From February 2023 to March 2023, 228 subjects were screened, and 225 were randomized. The HT and BQT groups showed eradication rates of 76.3% and 61.3% ( p = 0.015) both by intention-to-treat (ITT) analysis and per-protocol (PP) analysis. HT was associated with fewer adverse events than BQT (27.2% vs. 81.8%, p = 0.002). The most commonly reported adverse events was bitter taste of mouth (3.5% vs. 60.4%, p < 0.001). There was no significant difference in compliance between the two groups (89.5% vs. 92.8%, p = 0.264). Conclusion: The 14-day HT treatment demonstrates better efficacy in H. pylori eradication treatment and improved safety and compliance compared to BQT. The results provide supporting evidence for 14-day HT can be potentially considered as a first-line regimen for empirical treatment. Clinical Trial Registration: https://www.chictr.org.cn/showproj.html?proj=186562 , identifier ChiCTR2200066284

Cite

Citation style:
Could not load citation form.

Access Statistic

Total:
Downloads:
Abtractviews:
Last 12 Month:
Downloads:
Abtractviews:

Rights

License Holder: Copyright © 2023 Cheng, Fan, Huang, Zhai, Wang, Xie, Cai, Li, Bai, Wang and Ding.

Use and reproduction: