Methods | Six-week randomised, double-blind multicentre study. | |
Participants | Outpatients fulfilling DSM-III criteria for major depressive disorder (with a duration of illness of at least 4 weeks), with a score of at least 20 on the HDRS-21 and a score of at least 8 on the Raskin. Age range: 18-70 years old. Exclusion criteria: not stated. |
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Interventions | Fluoxetine: 185 participants. Imipramine: 186 participants. Placebo: 169 participants. Fluoxetine dose range: 20-80 mg/day. Imipramine dose range: 75-300 mg/day. |
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Outcomes | Hamilton Rating Scale for Depression, Raskin Depression Scale, Covi Anxiety Scale, CGI-I and CGI-S | |
Notes | Funding: by industry | |
Risk of bias | ||
Item | Authors’ judgement | Description |
Allocation concealment? | Unclear | B - Unclear |