Publication:
Efficacy of etoricoxib 60 mg/day and diclofenac 150 mg/day in reduction of pain and disability in patients with chronic low back pain: Results of a 4-week, multinational, randomized, double-blind study

dc.contributor.authorC. Zerbinien_US
dc.contributor.authorZafer E. Ozturken_US
dc.contributor.authorJ. Grifkaen_US
dc.contributor.authorM. Mainien_US
dc.contributor.authorS. Nilganuwongen_US
dc.contributor.authorR. Moralesen_US
dc.contributor.authorM. Huplien_US
dc.contributor.authorM. Shivaprakashen_US
dc.contributor.authorH. Giezeken_US
dc.contributor.otherHeliopolis Hospitalen_US
dc.contributor.otherMerck & Co., Inc.en_US
dc.contributor.otherUniversitat Regensburgen_US
dc.contributor.otherIstituti Clinici Scientifici Maugeri Spa – Società benefiten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherClinica San Gabrielen_US
dc.contributor.otherSouth Karelia Central Hospitalen_US
dc.date.accessioned2018-06-21T08:20:26Z
dc.date.available2018-06-21T08:20:26Z
dc.date.issued2005-12-01en_US
dc.description.abstractBackground and methods: The efficacy and safety of etoricoxib 60 mg/day in patients with established chronic low back pain (CLBP) were compared with those of diclofenac 150 mg/day in a 4-week, multicentre, randomized, double-blind, parallel-group trial. Four hundred and forty-six adult patients with CLBP (Quebec Task Force on Spinal Disorders Class 1 or 2) and with worsening pain upon discontinuation of pre-study analgesic medication were enrolled in the study. The study primary efficacy endpoint was change from baseline in Low Back Pain Intensity Scale (LBP-IS) score over the 4-week treatment period. Secondary and other efficacy endpoints included: changes in Roland and Morris Disability Questionnaire (RMDQ), Patient Global Assessment of Response to Therapy (PGART) and Low Back Pain Bothersomeness Scale (LBP-BS) scores. Early efficacy was assessed using PGART and LBP-IS scores 4 h after the first dose on the mornings of Days 1, 2 and 3. The overall safety and tolerability of etoricoxib 60 mg/day during 4 weeks of treatment were also assessed. Results: The least-squares mean time-weighted change from baseline LBP-IS score over 4 weeks was -32.94mm (95% CI -36.25, -29.63) for etoricoxib, indicating substantial efficacy in relief of pain. The treatment difference for the primary outcome was 2.51 mm (95% CI -1.50, 6.51), fulfilling the prespecified equivalence criterion of 95% confidence interval wholly within ± 10 mm. Etoricoxib improved all secondary and other efficacy outcomes. There were no statistically significant between-group differences in the proportion of patients with one or more clinical adverse events (AEs) (etoricoxib 35%, diclofenac 39%), or the proportion of patients who discontinued due to AEs (etoricoxib 7%, diclofenac 5%). Conclusions: The results of this study confirm that, for adult patients with CLBP, etoricoxib 60 mg once daily over 4 weeks is effective for relief of pain and improvement of physical function and comparable to high-dose diclofenac 150 mg daily. © 2005 Librapharm Limited.en_US
dc.identifier.citationCurrent Medical Research and Opinion. Vol.21, No.12 (2005), 2037-2049en_US
dc.identifier.doi10.1185/030079905X75069en_US
dc.identifier.issn03007995en_US
dc.identifier.other2-s2.0-29144515507en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/16725
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=29144515507&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleEfficacy of etoricoxib 60 mg/day and diclofenac 150 mg/day in reduction of pain and disability in patients with chronic low back pain: Results of a 4-week, multinational, randomized, double-blind studyen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=29144515507&origin=inwarden_US

Files

Collections