Background. In the treatment of upper GI endoscopy-negative patients with heartburn and epigastric pain or burning, antacids, anti-reflux agents, and mucosal protective agents (MPA) are widely used, alone or as add-on treatment to increase response to proton pump inhibitors, which are not indicated in infancy and pregnancy, and account for significant cost expenditure. Aims & Methods: In this randomized, controlled, double-blind, double-dummy, multicenter trial assessing the efficacy and safety of MPA Poliprotect (neoBianacid®) versus Omeprazole in the relief of heartburn and epigastric pain/burning, 275 endoscopy-negative outpatients were given a 4-week treatment with Omeprazole (20 mg q.d.) or Poliprotect (5 times a day for the initial 2 weeks, and on-demand thereafter), followed by an open-label 4-week treatment period with Poliprotect on demand. Gut microbiota change was assessed.Results: A 2-week treatment with Poliprotect proved non-inferior to Omeprazole for symptom relief (between-group difference in the change in VAS symptom score: [mean, 95% CI] -5.4, -9.9 to -0.1; -6.2, -10.8 to -1.6; ITT and PP populations, respectively).Poliprotect’s benefit remained unaltered after shifting to on-demand intake, with no gut microbiota variation. The initial benefit of Omeprazole was maintained against significantly higher use of rescue medicine sachets (mean, 95% CI: Poliprotect 3.9, 2.8–5.0; Omeprazole 8.2, 4.8–11.6) and associated with an increased abundance of oral cavity genera in the intestinal microbiota. No relevant adverse events were reported in either treatment arm.
Poliprotect vs omeprazole in the relief of heartburn, epigastric pain and burning in patients without erosive esophagitis and gastro-duodenal lesions. A randomized, controlled trial / Corazziari, Enrico Stefano; Gasbarrini, Antonio; D’Alba, Lucia; D'Ovidio, Valeria; Riggio, Oliviero; Passaretti, Sandro; Annibale, Bruno; Cicala, Michele; Repici, Alessandro; Bassotti, Gabrio; Ciacci, Carolina; Di Sabatino, Antonio; Neri, Matteo; Bragazzi, MARIA CONSIGLIA; Ribichini, Emanuela; Radocchia, Giulia; Iovino, Paola; Marazzato, Massimiliano; Schippa, Serena; Badiali, Danilo. - In: THE AMERICAN JOURNAL OF GASTROENTEROLOGY. - ISSN 1572-0241. - .:.(2023), pp. 1-21. [10.14309/ajg.0000000000002360]
Poliprotect vs omeprazole in the relief of heartburn, epigastric pain and burning in patients without erosive esophagitis and gastro-duodenal lesions. A randomized, controlled trial
Enrico Stefano Corazziari
Primo
Conceptualization
;Valeria D’OvidioWriting – Review & Editing
;Oliviero RiggioWriting – Review & Editing
;Bruno AnnibaleWriting – Review & Editing
;Maria Consiglia Bragazzi;Emanuela Ribichini;Giulia RadocchiaInvestigation
;Massimiliano MarazzatoInvestigation
;Serena SchippaWriting – Original Draft Preparation
;Danilo BadialiUltimo
Writing – Original Draft Preparation
2023
Abstract
Background. In the treatment of upper GI endoscopy-negative patients with heartburn and epigastric pain or burning, antacids, anti-reflux agents, and mucosal protective agents (MPA) are widely used, alone or as add-on treatment to increase response to proton pump inhibitors, which are not indicated in infancy and pregnancy, and account for significant cost expenditure. Aims & Methods: In this randomized, controlled, double-blind, double-dummy, multicenter trial assessing the efficacy and safety of MPA Poliprotect (neoBianacid®) versus Omeprazole in the relief of heartburn and epigastric pain/burning, 275 endoscopy-negative outpatients were given a 4-week treatment with Omeprazole (20 mg q.d.) or Poliprotect (5 times a day for the initial 2 weeks, and on-demand thereafter), followed by an open-label 4-week treatment period with Poliprotect on demand. Gut microbiota change was assessed.Results: A 2-week treatment with Poliprotect proved non-inferior to Omeprazole for symptom relief (between-group difference in the change in VAS symptom score: [mean, 95% CI] -5.4, -9.9 to -0.1; -6.2, -10.8 to -1.6; ITT and PP populations, respectively).Poliprotect’s benefit remained unaltered after shifting to on-demand intake, with no gut microbiota variation. The initial benefit of Omeprazole was maintained against significantly higher use of rescue medicine sachets (mean, 95% CI: Poliprotect 3.9, 2.8–5.0; Omeprazole 8.2, 4.8–11.6) and associated with an increased abundance of oral cavity genera in the intestinal microbiota. No relevant adverse events were reported in either treatment arm.File | Dimensione | Formato | |
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Corazziari_Poliprotect_2023.pdf
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