A randomized, controlled, trial of controlled release paroxetine in Fibromyalgia

Journal: The American Journal of Medicine. 2007 May;120(5):448-54.

Authors and affiliation: Patkar AA, Masand PS, Krulewicz S, Mannelli P, Peindl K, Beebe KL, Jiang W. Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina, USA. [E-mail: ashwin.patkar@duke.edu ]

PMID: 17466657

Purpose: We investigated the efficacy and tolerability of paroxetine controlled release, a selective serotonin reuptake inhibitor in Fibromyalgia.

Methods: After excluding patients with current major depression and anxiety disorders, 116 subjects with Fibromyalgia were enrolled in a 12-week, randomized, double-blind, placebo-controlled, trial of paroxetine controlled release (12.5-62.5 mg/day). The primary outcome measure was proportion of responders as defined as a> or =25% reduction in scores on the Fibromyalgia Impact Questionnaire (FIQ) from randomization to end of treatment. Secondary outcome measures included changes in FIQ scores, Clinical Global Impression -Improvement (CGI-I) and Severity (CGI-S) scores, Visual Analogue Scale for pain scores, number of tender points, and scores on the Sheehan Disability Scale (SDS).


n Significantly more patients in paroxetine controlled release group (57%) showed a> or =25% reduction in FIQ compared to placebo (33%) (P=.016).

n Paroxetine controlled release was significantly superior to placebo in reducing the FIQ total score (P =.015).

n The CGI-I ratings significantly favored the drug over placebo (P<.005).

n The improvements on other secondary outcome measures between the 2 groups were not statistically significant. Drowsiness, dry mouth, blurred vision, genital disorders, and anxiety were reported more frequently with paroxetine controlled release.

The mean dose of paroxetine controlled release was 39.1 mg/day.

Conclusions: Paroxetine controlled release appears to be well-tolerated and improve the overall symptomatology in patients with Fibromyalgia without current mood or anxiety disorders. However, its effect on pain measures seems to be less robust.

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