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Alternative vs. conventional treatment given on-demand for gastroesophageal reflux disease: a randomised controlled trial

BACKGROUND: Alternative treatments are commonly used for various disorders and often taken on-demand. On-demand treatment of gastroesophageal reflux disease (GERD) with pharmaceutical products is an established, cost-effective strategy. Comparisons between alternative medicine and pharmaceutical pro...

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Autores principales: Farup, Per G, Heibert, Mathis, Høeg, Victor
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657103/
https://www.ncbi.nlm.nih.gov/pubmed/19236727
http://dx.doi.org/10.1186/1472-6882-9-3
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author Farup, Per G
Heibert, Mathis
Høeg, Victor
author_facet Farup, Per G
Heibert, Mathis
Høeg, Victor
author_sort Farup, Per G
collection PubMed
description BACKGROUND: Alternative treatments are commonly used for various disorders and often taken on-demand. On-demand treatment of gastroesophageal reflux disease (GERD) with pharmaceutical products is an established, cost-effective strategy. Comparisons between alternative medicine and pharmaceutical products are rare. The aim of this trial was to compare on-demand treatment with a pectin-based, raft-forming, natural, anti-reflux agent (PRA) with that of esomeprazole 20 mg (Eso20) in patients with mild/moderate GERD. METHODS: Patients with mild/moderate GERD were randomised to a six weeks' on-demand treatment with PRA or Eso20 in a pragmatic, open, multicentre trial. Overall satisfaction with treatment, satisfactory relief on a weekly basis, reflux symptoms, and treatment preferences were noted. RESULTS: Seventy-seven patients were included in the analyses. Eso20 was significantly superior to PRA for proportion of overall satisfied patients (92% and 58% respectively; p = 0.001), reduction of symptoms (mean symptom scores at the end 5.9 and 8.0 respectively; p = 0.019), proportion of weeks of satisfactory relief (89% and 62% respectively; p = 0.008) and proportion preferring continuation with the same treatment (85% and 42% respectively; p < 0.001). Older patients were more satisfied than younger, and patients preferring on-demand treatment had lower symptom scores at inclusion than those preferring regular treatment. CONCLUSION: On-demand treatment with esomeprazole 20 mg was clearly superior to the pectin-based raft-forming agent. Most patients preferred on-demand treatment to regular treatment. Those preferring regular therapy had significantly more symptoms at inclusion. TRIAL REGISTRATION: ClinicalTrials.gov: NCT00184522.
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spelling pubmed-26571032009-03-18 Alternative vs. conventional treatment given on-demand for gastroesophageal reflux disease: a randomised controlled trial Farup, Per G Heibert, Mathis Høeg, Victor BMC Complement Altern Med Research Article BACKGROUND: Alternative treatments are commonly used for various disorders and often taken on-demand. On-demand treatment of gastroesophageal reflux disease (GERD) with pharmaceutical products is an established, cost-effective strategy. Comparisons between alternative medicine and pharmaceutical products are rare. The aim of this trial was to compare on-demand treatment with a pectin-based, raft-forming, natural, anti-reflux agent (PRA) with that of esomeprazole 20 mg (Eso20) in patients with mild/moderate GERD. METHODS: Patients with mild/moderate GERD were randomised to a six weeks' on-demand treatment with PRA or Eso20 in a pragmatic, open, multicentre trial. Overall satisfaction with treatment, satisfactory relief on a weekly basis, reflux symptoms, and treatment preferences were noted. RESULTS: Seventy-seven patients were included in the analyses. Eso20 was significantly superior to PRA for proportion of overall satisfied patients (92% and 58% respectively; p = 0.001), reduction of symptoms (mean symptom scores at the end 5.9 and 8.0 respectively; p = 0.019), proportion of weeks of satisfactory relief (89% and 62% respectively; p = 0.008) and proportion preferring continuation with the same treatment (85% and 42% respectively; p < 0.001). Older patients were more satisfied than younger, and patients preferring on-demand treatment had lower symptom scores at inclusion than those preferring regular treatment. CONCLUSION: On-demand treatment with esomeprazole 20 mg was clearly superior to the pectin-based raft-forming agent. Most patients preferred on-demand treatment to regular treatment. Those preferring regular therapy had significantly more symptoms at inclusion. TRIAL REGISTRATION: ClinicalTrials.gov: NCT00184522. BioMed Central 2009-02-24 /pmc/articles/PMC2657103/ /pubmed/19236727 http://dx.doi.org/10.1186/1472-6882-9-3 Text en Copyright © 2009 Farup et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Farup, Per G
Heibert, Mathis
Høeg, Victor
Alternative vs. conventional treatment given on-demand for gastroesophageal reflux disease: a randomised controlled trial
title Alternative vs. conventional treatment given on-demand for gastroesophageal reflux disease: a randomised controlled trial
title_full Alternative vs. conventional treatment given on-demand for gastroesophageal reflux disease: a randomised controlled trial
title_fullStr Alternative vs. conventional treatment given on-demand for gastroesophageal reflux disease: a randomised controlled trial
title_full_unstemmed Alternative vs. conventional treatment given on-demand for gastroesophageal reflux disease: a randomised controlled trial
title_short Alternative vs. conventional treatment given on-demand for gastroesophageal reflux disease: a randomised controlled trial
title_sort alternative vs. conventional treatment given on-demand for gastroesophageal reflux disease: a randomised controlled trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657103/
https://www.ncbi.nlm.nih.gov/pubmed/19236727
http://dx.doi.org/10.1186/1472-6882-9-3
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