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dc.contributor.author강창남-
dc.date.accessioned2021-03-26T04:41:00Z-
dc.date.available2021-03-26T04:41:00Z-
dc.date.issued2020-01-
dc.identifier.citationPLOS ONE, v. 15, no. 1, article no. e0226184en_US
dc.identifier.issn1932-6203-
dc.identifier.urihttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0226184-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/160886-
dc.description.abstractObjective Selective cyclooxygenase-2 inhibitors (celecoxib) can minimize the gastrointestinal complications related to non-steroidal anti-inflammatory drug (NSAID) use. NAXOZOL is a new combination formulation designed to provide sequential delivery of a non-enteric-coated, immediate-release esomeprazole strontium tetrahydrate 20 mg mantle followed by an enteric-coated naproxen 500 mg core. However, there have been no studies comparing NAXOZOL to celecoxib with respect to gastrointestinal tract protection and pain relief in patients with osteoarthritis. This study was undertaken to compare the effects of NAXOZOL and celecoxib with respect to gastrointestinal tract protection and pain relief in patients with osteoarthritis. Methods The randomized enrolled patients were divided into two treatment groups: a NAXOZOL group and a celecoxib group. All participants received treatments (NAXOZOL, 500/20 mg (naproxen 500 mg, esomeprazole strontium tetrahydrate 20 mg) twice per day versus celecoxib, 200 mg daily) on a 1:1 allocation basis for 12 weeks. The primary outcome was the Leeds Dyspepsia Questionnaire (LDQ) score used for non-inferiority testing. Secondary outcome measures included the Gastrointestinal Symptom Rating Scale (GSRS) score, Visual Analogue Scale (VAS) score, European Quality of Life-5 dimensions (EQ-5D) scale and the EQ-5D Visual Analogue Scale (EQ VAS). Other outcome measures included the use of supplementary or rescue drugs, and the incidence of adverse events. Results The baseline-adjusted LDQ scores immediately after 12 weeks of treatment in NAXOZOL group were not inferior to those in celecoxib group. The overall change in the baselineadjusted GSRS score, VAS score, EQ-5D, and EQ VAS was not different between the two groups. The usage of supplementary drugs and the drug-related incidence of adverse events were not different. However, the days to use rescue drug were longer in celecoxib group than in NAXOZOL group. Conclusion NAXOZOL was not inferior to celecoxib in protecting the gastrointestinal tract and providing pain relief in patients with osteoarthritis.en_US
dc.description.sponsorshipThis study was supported by a research fund from Hanmi Pharmaceutical Co., Ltd (grant number HM-IITNAX-001). NAXOZOL (R) (Naproxen, Esomeprazole strontium) was provided by Hanmi Pharmaceutical Co., Ltd. The funder provided support in the form of salaries for authors [MSP, CNK, WSL, HJK, SHL, JHK, SJS, SHM], but did not have any additional role in the study design, data collection, and analysis, decision to publish, or preparation of the manuscript. The funder was not involved in any part of the trial implementation or data analysis. The specific roles of these authors are articulated in the `author contributions' section.en_US
dc.language.isoenen_US
dc.publisherPUBLIC LIBRARY SCIENCEen_US
dc.subjectFIXED-DOSE COMBINATIONen_US
dc.subjectESOMEPRAZOLE MAGNESIUMen_US
dc.subjectCLINICAL-TRIALen_US
dc.subjectGASTROINTESTINAL TOLERABILITYen_US
dc.subjectNONSPECIFIC NSAIDSen_US
dc.subjectCOX-2 INHIBITORSen_US
dc.subjectADVERSE EVENTSen_US
dc.subjectNAPROXENen_US
dc.subjectSYMPTOMSen_US
dc.subjectPREVENTIONen_US
dc.titleA comparative study of the efficacy of NAXOZOL compared to celecoxib in patients with osteoarthritisen_US
dc.typeArticleen_US
dc.identifier.doi10.1371/journal.pone.0226184-
dc.relation.page1-14-
dc.relation.journalPLOS ONE-
dc.contributor.googleauthorPark, Moon Soo-
dc.contributor.googleauthorKang, Chang-Nam-
dc.contributor.googleauthorLee, Woo-Suk-
dc.contributor.googleauthorKim, Ho-Joong-
dc.contributor.googleauthorLee, Sahnghoon-
dc.contributor.googleauthorKim, Jin Hwan-
dc.contributor.googleauthorShin, Sang-Jin-
dc.contributor.googleauthorMoon, Seong-Hwan-
dc.relation.code2020046504-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidcnkang65-


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