Methods | Six-week randomised, double-blind study. | |
Participants | Inpatients fulfilling Research Diagnostic Criteria for major depressive disorder, with a score of at least 17 on the HDRS. Age range: 18-64 years old. Exclusion criteria: concurrent medical disorder. |
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Interventions | Fluoxetine: 16 participants. Amitriptyline : 18 participants. Fluoxetine dose range: 40-60 mg/day. Amitriptyline dose range: 100-150 mg/day. Only oxazepam (max 100 mg/day) was allowed. |
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Outcomes | Hamilton Rating Scale for Depression, Montgomery and Asberg Scale for Depression (MADRS), CGI Severity and Improvement, PGI, | |
Notes | Funding: by industry | |
Risk of bias | ||
Item | Authors’ judgement | Description |
Allocation concealment? | Unclear | B - Unclear |