Valdecoxib, a
cyclooxygenase (COX)-2 specific inhibitor, is indicated for relief of the signs and symptoms of
rheumatoid arthritis,
osteoarthritis, and primary
dysmenorrhea. Therapeutic doses of COX-2 specific inhibitors are as effective as nonspecific nonsteroidal anti-inflammatory drugs in reducing inflammatory
pain while sparing the gastrointestinal and platelet toxicity associated with nonspecific COX-1 inhibition.
OBJECTIVE: This 4-week, prospective, randomized, double-blind placebo-controlled, parallel-group study was conducted at 37 centers across the United States and 5 centers in Canada. Patients aged > or =18 years with chronic
low back pain in flare were enrolled. Patients were randomized to receive
valdecoxib 40-mg/d or placebo
tablets, once daily for 4 weeks. Patients rated
low back pain intensity on a visual analog scale and completed the Roland-Morris Disability Questionnaire and the modified Brief
Pain Inventory-Short Form (mBPI-SF) at each visit.
RESULTS: Two hundred ninety-three patients were enrolled. The
valdecoxib group comprised 148 patients (81 women, 67 men; mean [SD] age, 48.6 [13.3] years; mean [SD]
body weight, 86.6 [20.9] kg), and the placebo group included 145 patients (85 women, 60 men; mean [SD] age, 48.7 [12.6] years; mean [SD]
body weight, 85.6 [19.9] kg). Of the enrolled patients, 249 completed the study: 134 patients (91%) who received
valdecoxib and 115 patients (79%) who received placebo. No statistically significant differences in patient baseline characteristics were noted between treatment groups, except in response to 1 mBPI-SF question; patients in the
valdecoxib group reported significantly greater interference in relations with other people due to
pain than did those in the placebo group (P = 0.048). Changes from baseline in
low back pain intensity were significantly greater in
valdecoxib-treated patients at each assessment (all, P < 0.001 vs placebo).
Pain scores on the mBPI-SF indicated significantly greater
pain relief with
valdecoxib at each assessment (all, P < or = 0.014 vs placebo). Improvements in mean Roland-Morris Disability Questionnaire score with
valdecoxib were significantly greater than with placebo at each assessment (all, P < or = 0.003). Although the overall incidence of adverse events (AEs) was significantly higher among patients receiving
valdecoxib than those receiving placebo (35.1% vs 24.1%, respectively; P = 0.042), no significant differences were found between groups for the incidence of any individual AE. Most AEs (89% [77/87 total events]) were mild or moderate in severity.
CONCLUSIONS: