Fluoxetine in the acute treatment and relapse prevention of combat-related post-traumatic stress disorder: Analysis of the veteran group of a placebo-controlled, randomized clinical trial

The efficacy and safety of fluoxetine (20–80 mg) was compared with placebo in 144 veterans [36.2 years], diagnosed with combat-related post-traumatic stress disorder (PTSD) selected from a 12-week acute and 24-week relapse prevention PTSD trial. In the acute phase, improvements were greater with flu...

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Bibliographic Details
Published inEuropean neuropsychopharmacology Vol. 16; no. 5; pp. 340 - 349
Main Authors Martenyi, Ferenc, Soldatenkova, Victoria
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.07.2006
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