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 |
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Interventions | Fluoxetine: 29 participants. Imipramine: 30 participants. Fluoxetine dose: 20 mg/day. Imipramine dose range: 75-150 mg/day. |
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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 |