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. Author manuscript; available in PMC: 2014 Sep 15.
Published in final edited form as: Cochrane Database Syst Rev. 2005 Oct 19;(4):CD004185. doi: 10.1002/14651858.CD004185.pub2
Methods Eight-week double-blind, randomised study.
Participants Outpatients fulfilling DSM-III and Bech-Rafaelsen Melancholia Scale criteria for major depressive disorder, with a score of at least 18 on the HDRS-21.
Age range: 18-70 years old.
Exclusion criteria: suicide risk, history of schizophrenia or organic brain disfunction, history of severe allergies or serious physical illness, recent period of alcohol or alcohol abuse, pregnancy
Interventions Fluoxetine: 29 participants.
Imipramine: 30 participants.
Fluoxetine dose: 20 mg/day.
Imipramine dose range: 75-150 mg/day.
Outcomes Hamilton Rating Scale for Depression (HDRS-21), Bech-Rafaelsen Melancholia Scale, CGI, PGI
Notes Funding: by industry
Risk of bias
Item Authors’ judgement Description
Allocation concealment? Unclear B - Unclear