Open label, non-comparative, prospective study to evaluate cognitive functioning in remitted depression outpatients during long-term preventive treatment with Fluvoxamine (Fevarin®)
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
50
The subjects will be prescribed Fluvoxamine treatment for 24 weeks with dose 50-300 mg
Moscow Research Institution of Psychiatry
Moscow, Russia
Change of time difference between Part I and Part II of Stroop Test
Time frame: From baseline up to Week 24
Change of total Frontal Assessment Battery score
Time frame: From baseline up to Week 24
Proportion of patients maintained remission status
Time frame: Week 24
Changes of Addenbrooke's Cognitive Examination general score
Time frame: From baseline up to Week 24
Change of The Social Adaptation Self-evaluation Scale total score
Time frame: From baseline up to Week 24
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