Methods | Five-week randomised, double-blind study. | |
Participants | Outpatients with depressive syndrome with a score of at least 17 on the HDRS and 8 on the Raskin. Age range: 19-74 years old. Exclusion criteria: severe organic illness, evidence of psychosis, psychopathic disorder, addictive illness, suicide tendencies, a period of less than 4 weeks since the last treatment with amitriptyline or neuroleptics |
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Interventions | Fluoxetine: 63 participants. Amitriptyline : 65 participants. Fluoxetine dose range: 20-60 mg/day. Amitriptyline dose range: 50-150 mg/day. Chloral derivative was allowed (eventually changed in flurazepam or nitrazepam only if its effects was inadequate) |
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Outcomes | Hamilton Rating Scale for Depression (HDRS), CGI, Raskin Depression Scale, Covi Anxiety Scale, PGI | |
Notes | Funding: unclear | |
Risk of bias | ||
Item | Authors’ judgement | Description |
Allocation concealment? | Unclear | B - Unclear |