Methods | Six-week randomised, double-blind study. | |
Participants | In- and outpatients fulfilling DSM-III-R criteria for major depressive disorder (lasting 1 month or more), with a score of at least 20 on the HDRS-21. Age range: 18-65 years old. Exclusion criteria: any abnormalities on laboratory examination, presence of psychosis, bipolar disorder, conscurrent use of any psychoactive medication, pregnancy, lactation |
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Interventions | Fluoxetine: 26 participants. Desipramine: 20 participants. Fluoxetine dose range: 20-60 mg/day. Desipramine dose range: 150-300 mg/day. |
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Outcomes | Hamilton Rating Scale for Depression, CGI, PGI. | |
Notes | Funding: by industry | |
Risk of bias | ||
Item | Authors’ judgement | Description |
Allocation concealment? | Unclear | B - Unclear |