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.author | C. Zerbini | en_US |
dc.contributor.author | Zafer E. Ozturk | en_US |
dc.contributor.author | J. Grifka | en_US |
dc.contributor.author | M. Maini | en_US |
dc.contributor.author | S. Nilganuwong | en_US |
dc.contributor.author | R. Morales | en_US |
dc.contributor.author | M. Hupli | en_US |
dc.contributor.author | M. Shivaprakash | en_US |
dc.contributor.author | H. Giezek | en_US |
dc.contributor.other | Heliopolis Hospital | en_US |
dc.contributor.other | Merck & Co., Inc. | en_US |
dc.contributor.other | Universitat Regensburg | en_US |
dc.contributor.other | Istituti Clinici Scientifici Maugeri Spa – Società benefit | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.contributor.other | Clinica San Gabriel | en_US |
dc.contributor.other | South Karelia Central Hospital | en_US |
dc.date.accessioned | 2018-06-21T08:20:26Z | |
dc.date.available | 2018-06-21T08:20:26Z | |
dc.date.issued | 2005-12-01 | en_US |
dc.description.abstract | Background 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.citation | Current Medical Research and Opinion. Vol.21, No.12 (2005), 2037-2049 | en_US |
dc.identifier.doi | 10.1185/030079905X75069 | en_US |
dc.identifier.issn | 03007995 | en_US |
dc.identifier.other | 2-s2.0-29144515507 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/16725 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=29144515507&origin=inward | en_US |
dc.subject | Medicine | en_US |
dc.title | 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 | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=29144515507&origin=inward | en_US |