Publication:
A multicenter, randomized, prospective study of 14-day ranitidine bismuth citrate- vs. lansoprazole-based triple therapy for the eradication of Helicobacter pylori in dyspeptic patients

dc.contributor.authorKOCAKAYA, OZAN
dc.contributor.authorsAvsar, Erol; Tiftikci, Arzu; Poturoglu, Sule; Erzin, Yusuf; Kocakaya, Ozan; Dincer, Dinc; Yildirim, Bulut; Guliter, Sefa; Turkay, Cansel; Yilmaz, Ugur; Onuk, Mehmet Derya; Bolukbas, Cengiz; Ellidokuz, Ender; Bektas, Ahmet; Tasan, Guralp; Aytug, Necip; Ates, Yuksel; Kaymakoglu, Sabahattin
dc.date.accessioned2022-03-13T12:44:29Z
dc.date.accessioned2026-01-11T17:15:56Z
dc.date.available2022-03-13T12:44:29Z
dc.date.issued2013
dc.description.abstractBackground/aims: Proton-pump inhibitor- and ranitidine bismuth citrate-based triple regimens are the two recommended first-line treatments for the eradication of Helicobacter pylori. We aimed to compare the effectiveness and tolerability of these two treatments in a prospective, multi-centric, randomized study. Materials and Methods: Patients with dyspeptic complaints were recruited from 15 study centers. Presence of Helicobacter pylori was investigated by both histology and rapid urease test. The patients were randomized to either ranitidine bismuth citrate 400 mg bid plus amoxicillin 1 g bid plus clarithromycin 500 mg bid (n=149) or lansoprazole 30 mg bid plus amoxicillin 1 g bid plus clarithromycin 500 mg bid (n=130) treatment arm for 14 days. Adverse events have been recorded during the treatment phase. A C-13 urea breath test was performed 6 weeks after termination of treatment to assess the efficacy of the therapy. Eradication rate was calculated by intention-to-treat and per-protocol analysis. Results: Two hundred seventy-nine patients (123 male, 156 female) were eligible for randomization. In per-protocol analysis (n=247), Helicobacter pylori was eradicated with ranitidine bismuth citrate- and lansoprazole-based regimens in 74,6% and 69,2% of cases, respectively (p>0,05). Intention-to-treat analysis (n=279) revealed that eradication rates were 65,1% and 63,6% in ranitidine bismuth citrate- and in lansoprazole-based regimens, respectively (p>0,05). Both regimes were well-tolerated, and no serious adverse event was observed during the study. Conclusion: Ranitidine bismuth citrate-based regimen is at least as effective and tolerable as the classical proton-pump inhibitor-based regimen, but none of the therapies could achieve the recommendable eradication rate.
dc.identifier.doi10.4318/tjg.2013.0509
dc.identifier.issn1300-4948
dc.identifier.pubmed24254262
dc.identifier.urihttps://hdl.handle.net/11424/237543
dc.identifier.wosWOS:000326481900003
dc.language.isoeng
dc.publisherTURKISH SOC GASTROENTEROLOGY
dc.relation.ispartofTURKISH JOURNAL OF GASTROENTEROLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectRanitidine bismuth citrate
dc.subjectlansoprazole
dc.subjectHelicobacter pylori
dc.subjecteradication
dc.subjectDUODENAL-ULCER
dc.subject2 ANTIBIOTICS
dc.subjectCLARITHROMYCIN
dc.subjectINFECTION
dc.subjectAMOXICILLIN
dc.subjectOMEPRAZOLE
dc.subjectMANAGEMENT
dc.subjectRESISTANCE
dc.subjectRECURRENCE
dc.subjectBLIND
dc.titleA multicenter, randomized, prospective study of 14-day ranitidine bismuth citrate- vs. lansoprazole-based triple therapy for the eradication of Helicobacter pylori in dyspeptic patients
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage321
oaire.citation.issue4
oaire.citation.startPage316
oaire.citation.titleTURKISH JOURNAL OF GASTROENTEROLOGY
oaire.citation.volume24

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