Methods | Five-week randomised, double-blind study. | |
Participants | Patients fulfilling DSM-III criteria for major depressive episode, with a score of at least 18 on the first 17 items of the HDRS. Age range: 18-65 years old. Exclusion criteria: pregnancy, serious vascular disease, hyperthyroidism, glaucoma, urinary retention, hepatic, respiratory or renal marked failure, hematological disease, organic brain disease, seizures, alcohol and/or drug abuse |
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Interventions | Fluoxetine: 15 participants. Imipramine: 15 participants. Fluoxetine dose: 20 mg/day. Imipramine dose range: 100-150 mg/day. |
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Outcomes | Hamilton Rating Scale for Depression, CGI. | |
Notes | Funding: unclear | |
Risk of bias | ||
Item | Authors’ judgement | Description |
Allocation concealment? | Unclear | B - Unclear |