Methods | Six-week double-blind, randomised study. | |
Participants | Outpatients meeting DSM-IV diagnostic criteria for major depression, with a minimum baseline score of 20 on the HDRS-17. Age range: 19-54 years old. Exclusion criteria: any other psychiatric primary disease, current or past history of bipolar disorder, use of anxiolitic or MAOI or tryptophan, organic mental disorder, epilepsy, suicidal tendencies, any severe general disease, pregnancy, lactation |
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Interventions | Fluoxetine: 24 participants. Nortriptyline: 24 participants. Fluoxetine dose: 60 mg/day. Nortriptyline dose: 150 mg/day. |
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Outcomes | Primary outcome: Hamilton Rating Scale for Depression (HDRS-17) | |
Notes | Funding: unclear | |
Risk of bias | ||
Item | Authors’ judgement | Description |
Allocation concealment? | Unclear | B - Unclear |