Please use this identifier to cite or link to this item: https://repository.cihe.edu.hk/jspui/handle/cihe/1807
DC FieldValueLanguage
dc.contributor.authorSmith, Graeme Drummonden_US
dc.contributor.otherMitchell, S. A.-
dc.contributor.otherMee, A. S.-
dc.contributor.otherPalmer, K. R.-
dc.contributor.otherChapman, R. W.-
dc.date.accessioned2021-11-18T03:28:56Z-
dc.date.available2021-11-18T03:28:56Z-
dc.date.issued2002-
dc.identifier.urihttps://repository.cihe.edu.hk/jspui/handle/cihe/1807-
dc.description.abstractBackground: Alverine citrate has been used in the treatment of irritable bowel syndrome for many years. Aims: To compare the efficacy and safety of a new formulation of alverine citrate, a 120-mg capsule, with placebo given three times daily for 12 weeks. Methods: One hundred and seven patients with irritable bowel syndrome were entered into this three-centre, double-blind, randomized, placebo-controlled, parallel group trial. The primary end-point was relief of abdominal pain indicated by improvement in the scores for severity and frequency. Secondary efficacy variables included scores for other clinical symptoms and for overall well-being. Results: The severity and frequency of abdominal pain improved in 66% and 68% of patients treated with alverine citrate vs. 58% and 69% of the placebo group, but these differences were not significant. The mean percentage reduction in the scores for abdominal pain from baseline to the final assessment, although greater in the alverine citrate group (43.7%) compared with the placebo group (33.3%), was not statistically significant. Conclusions: Alverine citrate is no better than placebo at relieving the symptoms of irritable bowel syndrome. Future trials should be designed to take into account the high and persistent placebo response seen in this condition.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofAlimentary Pharmacology and Therapeuticsen_US
dc.titleAlverine citrate fails to relieve the symptoms of irritable bowel syndrome: Results of a double-blind, randomized, placebo-controlled trialen_US
dc.typejournal articleen_US
dc.identifier.doi10.1046/j.1365-2036.2002.01277.x-
dc.contributor.affiliationSchool of Health Sciencesen_US
dc.relation.issn1365-2036en_US
dc.description.volume16en_US
dc.description.issue6en_US
dc.description.startpage1187en_US
dc.description.endpage1195en_US
dc.cihe.affiliatedNo-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.cerifentitytypePublications-
item.openairetypejournal article-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.languageiso639-1en-
crisitem.author.deptSchool of Health Sciences-
crisitem.author.orcid0000-0003-2974-3919-
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