This is an assessment of the efficacy of venlafaxine-HCL augmentation with the neuroleptic quetiapine in treatment resistant depression.
We examine the efficacy of Venlafaxine-HCL augmentation with the neuroleptic Quetiapine in treatment resistant depression in a double-blind randomized clinical trial. Secondary objective is the evaluation of pharmacogenetic factors contributing to drug efficacy in treatment resistant depression.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
126
Venlafaxine XR up to 450 mg/d during the complete trial (8 weeks)
Quetiapine up to 200 mg/d for four weeks
Max Planck Institute of Psychiatry
Munich, Bavaria, Germany
Hamilton Depression Rating Scale (HDRS)
Time frame: after monotherapy and after augmentation
Self reported psychopathology (Beck Depression Inventory [BDI], State-Trait Anxiety Inventory [STAI])
Time frame: after monotherapy and after augmentation
Cognitive function
Time frame: after monotherapy and after augmentation
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