This is a Pilot Study to get a first indication whether Duloxetine may be effective for depressed patients with Atypical Features.
This Open Pilot Study will assess whether Duloxetine is effective for patients with Atypical Features. 20 patients having Major Depressive Disorder with Atypical Features or Dysthymic Disorder will receive Duloxetine in open fashion for 8 weeks. Dose will begin with 20 mg/d and increase to PDR maximal dose of 120 mg/d, if tolerated.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
20
Day 1-7: 20 mg/d; day 8-24: 30 mg/d; day 15-28: 60 mg/d; day 29-56: 120 mg/d. \* dose raises will occur only if pt. is tolerating the previous dose and not remitting.; dose may be lowered or increased in 30 mg increments if pt. has difficulty tolerating.
Depression Evaluation Service - New York State Psychiatric Institute
New York, New York, United States
Hamilton Depression Scale (HAM-D)
Time frame: 10 weeks
Atypical Depression Diagnostic Scale (ADDS)
Time frame: 10 weeks
Beck Depression Inventory (BDI)
Time frame: 10 weeks
Clinical Global Impression (CGI)
Time frame: 10 weeks
Patient Global Impression (PGI)
Time frame: 10 weeks
Inventory of Depressive Symptoms(IDS)
Time frame: 10 weeks
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