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Pregabalin in the treatment of post‐traumatic peripheral neuropathic pain: a randomized double‐blind trial
Author(s) -
Van Seventer R.,
Bach F. W.,
Toth C. C.,
Serpell M.,
Temple J.,
Murphy T. K.,
Nimour M.
Publication year - 2010
Publication title -
european journal of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 124
eISSN - 1468-1331
pISSN - 1351-5101
DOI - 10.1111/j.1468-1331.2010.02979.x
Subject(s) - pregabalin , medicine , placebo , neuropathic pain , anesthesia , adverse effect , anxiety , randomized controlled trial , discontinuation , sleep disorder , insomnia , psychiatry , alternative medicine , pathology
Background:  Pregabalin is effective in the treatment of peripheral and central neuropathic pain. This study evaluated pregabalin in the treatment of post‐traumatic peripheral neuropathic pain (including post‐surgical). Methods:  Patients with a pain score ≥4 (0–10 scale) were randomized and treated with either flexible‐dose pregabalin 150–600 mg/day ( n  = 127) or placebo ( n  = 127) in an 8‐week double‐blind treatment period preceded by a 2‐week placebo run‐in. Results:  Pregabalin was associated with a significantly greater improvement in the mean end‐point pain score vs. placebo; mean treatment difference was −0.62 (95% CI −1.09 to −0.15) ( P  =   0.01). The average pregabalin dose at end‐point was ∼326 mg/day. Pregabalin was also associated with significant improvements from baseline in pain‐related sleep interference, and the Medical Outcomes Study sleep scale sleep problems index and sleep disturbance subscale (all P  <   0.001). In the all‐patient group (ITT), pregabalin was associated with a statistically significant improvement in the Hospital Anxiety and Depression Scale anxiety subscale ( P  <   0.05). In total, 29% of patients had moderate/severe baseline anxiety; treatment with pregabalin in this subset did not significantly improve anxiety. More patients reported global improvement at end‐point with pregabalin than with placebo (68% vs. 43%; overall P  < 0.01). Adverse events led to discontinuation of 20% of patients from pregabalin and 7% from placebo. Mild or moderate dizziness and somnolence were the most common adverse events in the pregabalin group. Conclusion:  Flexible‐dose pregabalin 150–600 mg/day was effective in relieving neuropathic pain, improving disturbed sleep, improving overall patient status, and was generally well tolerated in patients with post‐traumatic peripheral neuropathic pain.

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