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Please use this identifier to cite or link to this item: https://hdl.handle.net/11055/572
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dc.contributor.authorBouroubi Aen_US
dc.contributor.authorDonazzolo Yen_US
dc.contributor.authorDonath Fen_US
dc.contributor.authorEccles Ren_US
dc.contributor.authorRusso Men_US
dc.contributor.authorHarambillet Nen_US
dc.contributor.authorGautier Sen_US
dc.contributor.authorMontagne Aen_US
dc.date2017-09-04-
dc.date.accessioned2018-06-15T01:03:55Z-
dc.date.available2018-06-15T01:03:55Z-
dc.date.issued2017-09-04-
dc.identifier.citation71(9):e12961en_US
dc.identifier.urihttp://hdl.handle.net/11055/572-
dc.description.abstractOBJECTIVE: The aim of this study was to compare the efficacy and safety of a new oromucosal ibuprofen form, ibuprofen 25 mg lozenge, in single and repeat dosing for up to 4 days, to the matched placebo, in the treatment of acute sore throat pain in adults. METHODS: In this randomised, double-blind, placebo-controlled trial, adult patients with non-streptococcal sore throat and signs of moderate-to-severe associated pain (≥5 on the objective Tonsillo-Pharyngitis Assessment 21-point scale and ≥60 mm on the subjective 0-100 mm visual analogue Sore Throat Pain Intensity Scale [STPIS]) were assigned ibuprofen 25 mg (n=194) or matching placebo (n=191) lozenge treatment. Efficacy was assessed (at the investigating centre up to 2 hours after first dosing, then on an ambulatory basis) by parameters derived from patient's scores on scales of pain relief, pain intensity, and global efficacy assessment. The primary efficacy end-point was the time-weighted TOTal PAin Relief (TOTPAR) over 2 hours after first dosing using the Sore Throat Relief Scale (STRS). Safety and local tolerability were assessed. RESULTS: Ibuprofen 25 mg was superior to placebo on numerous pain relief parameters; TOTPAR was significantly higher with ibuprofen 25 mg over 2 hours after first dosing (P<.05), the effect being apparent from the first evaluation at 15 minutes (P<.05). The STPIS reduction in favour of ibuprofen 25 mg was not significant vs placebo. Mean STRS scores and patient's global efficacy assessment both reflected a higher efficacy of ibuprofen 25 mg over the 4-day treatment period with tests of statistical significance up to day 1 evening (P<.05), and, in patients with still clinically significant pain (n=128), after an average 4 days (P<.01). Ibuprofen 25 mg lozenge was well tolerated with a safety profile similar to placebo. CONCLUSION: Low-dose ibuprofen 25 mg lozenge in repeat dosing provides in adults more efficacious and rapid relief of sore throat pain and is as well tolerated as placebo.en_US
dc.subjectsore throaten_US
dc.subjectpain reliefen_US
dc.subjectlozengeen_US
dc.subjectibuprofenen_US
dc.subjectpharyngitisen_US
dc.titlePain relief of sore throat with a new anti-inflammatory throat lozenge, ibuprofen 25 mg: A randomised, double-blind, placebo-controlled, international phase III studyen_US
dc.typeJournal Articleen_US
dc.type.contentTexten_US
dc.identifier.journaltitleInternational Journal of Clinical Practiceen_US
dc.identifier.doi10.1111/ijcp.12961en_US
dc.description.affiliatesCentre de Recherche et Développement Pierre Fabre, Toulouse, Franceen_US
dc.description.affiliatesEurofins Optimed, Gières, Franceen_US
dc.description.affiliatesSocraTec R&D GmbH, Oberursel, Germanyen_US
dc.description.affiliatesCommon Cold Centre, Cardiff University, Cardiff, UKen_US
dc.description.affiliatesHunter Pain Clinic, Newcastle, New South Wales, Australiaen_US
dc.description.pubmedurihttps://www.ncbi.nlm.nih.gov/pubmed/28869722en_US
dc.type.studyortrialRandomized Controlled Clinical Trial/Controlled Clinical Trialen_US
dc.identifier.studynameNCT01785862en_US
dc.ispartof.anzcaresearchfoundationYesen_US
local.message.claim2023-05-02T12:05:54.601+1000|||rp00166|||submit_approve|||dc_contributor_author|||None*
dc.type.specialtyAnaesthesiaen_US
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
item.grantfulltextreserved-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
Appears in Collections:Scholarly and Clinical
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