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J Int Med Res ; 37(6): 1789-802, 2009.
Article de Anglais | MEDLINE | ID: mdl-20146877

RÉSUMÉ

Two 6-week studies compared the analgesic efficacy, tolerability and safety of a non-steroidal anti-inflammatory drug (celecoxib 200 mg twice a day [bid]) and an opioid (tramadol HCl 50 mg four times a day [qid]) in subjects with chronic low-back pain (CLBP). Successful responders (primary endpoint) were defined as subjects completing 6 weeks of treatment and having > or = 30% improvement on the Numerical Rating Scale for pain. A total of 796 and 802 subjects were randomized to treatment in study 1 and study 2, respectively. A significantly greater percentage of celecoxib-treated subjects were successful responders compared with tramadol HCl-treated subjects (study 1: 63.2% versus 49.9%, respectively; study 2: 64.1% versus 55.1%, respectively). Fewer adverse events (AEs) and serious AEs were reported in the celecoxib-treated group. Overall, celecoxib 200 mg bid was more effective than tramadol HCl 50 mg qid in the treatment of CLBP, with fewer AEs reported.


Sujet(s)
Inhibiteurs de la cyclooxygénase 2/effets indésirables , Inhibiteurs de la cyclooxygénase 2/usage thérapeutique , Lombalgie/traitement médicamenteux , Pyrazoles/effets indésirables , Pyrazoles/usage thérapeutique , Sulfonamides/effets indésirables , Sulfonamides/usage thérapeutique , Tramadol/effets indésirables , Tramadol/usage thérapeutique , Adolescent , Adulte , Sujet âgé , Analgésiques morphiniques/effets indésirables , Analgésiques morphiniques/usage thérapeutique , Anti-inflammatoires non stéroïdiens/effets indésirables , Anti-inflammatoires non stéroïdiens/usage thérapeutique , Causalité , Célécoxib , Maladie chronique , Démographie , Méthode en double aveugle , Femelle , Humains , Mâle , Adulte d'âge moyen , Résultat thérapeutique , Jeune adulte
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