TY - JOUR
T1 - Paroxetine in social phobia/social anxiety disorder
T2 - Randomised, double- blind, placebo-controlled study
AU - Baldwin, David
AU - Bobes, Julio
AU - Stein, Dan J.
AU - Scharwächter, Ingebor
AU - Faure, Michel
PY - 1999
Y1 - 1999
N2 - Background: Preliminary studies have suggested that paroxetine may be effective in social phobia/social anxiety disorder. Aims: To assess the efficacy and tolerability of paroxetine in the acute (12-week) treatment of social phobia. Method: Two-hundred and ninety patients with social phobia were assigned randomly to paroxetine (20-50 mg/day flexible dose) or placebo for 12 weeks of double-blind treatment. Primary efficacy outcomes were the Liebowitz Social Anxiety Scale (LSAS) total score (patient-rated) and the Clinical Global Impression (CGI) scale global improvement item. The secondary efficacy variables included CGI scale severity of illness score and the patient-rated Social Avoidance and Distress Scale. Results: Paroxetine produced a significantly greater reduction in LSAS total score (mean change from baseline: - 29.4 v. -15.6; P ≤ 0.001) and a greater proportion of responders (score ≤ 2 on CGI global improvement) (65.7% v. 32.4%; P<0.001) compared with placebo at the end of the 12-week study period. Both primary efficacy variables were statistically significant compared with placebo from week 4 onwards. Paroxetine was generally well tolerated. Conclusions: Paroxetine is an effective, well-tolerated treatment for patients with social phobia. Declaration: of interest Smith Kline Beecham Pharmaceuticals provided financial support for this study.
AB - Background: Preliminary studies have suggested that paroxetine may be effective in social phobia/social anxiety disorder. Aims: To assess the efficacy and tolerability of paroxetine in the acute (12-week) treatment of social phobia. Method: Two-hundred and ninety patients with social phobia were assigned randomly to paroxetine (20-50 mg/day flexible dose) or placebo for 12 weeks of double-blind treatment. Primary efficacy outcomes were the Liebowitz Social Anxiety Scale (LSAS) total score (patient-rated) and the Clinical Global Impression (CGI) scale global improvement item. The secondary efficacy variables included CGI scale severity of illness score and the patient-rated Social Avoidance and Distress Scale. Results: Paroxetine produced a significantly greater reduction in LSAS total score (mean change from baseline: - 29.4 v. -15.6; P ≤ 0.001) and a greater proportion of responders (score ≤ 2 on CGI global improvement) (65.7% v. 32.4%; P<0.001) compared with placebo at the end of the 12-week study period. Both primary efficacy variables were statistically significant compared with placebo from week 4 onwards. Paroxetine was generally well tolerated. Conclusions: Paroxetine is an effective, well-tolerated treatment for patients with social phobia. Declaration: of interest Smith Kline Beecham Pharmaceuticals provided financial support for this study.
UR - http://www.scopus.com/inward/record.url?scp=0032773913&partnerID=8YFLogxK
U2 - 10.1192/bjp.175.2.120
DO - 10.1192/bjp.175.2.120
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C2 - 10627793
AN - SCOPUS:0032773913
SN - 0007-1250
VL - 175
SP - 120
EP - 126
JO - British Journal of Psychiatry
JF - British Journal of Psychiatry
IS - AUG.
ER -