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. Author manuscript; available in PMC: 2014 Sep 15.
Published in final edited form as: Cochrane Database Syst Rev. 2005 Oct 19;(4):CD004185. doi: 10.1002/14651858.CD004185.pub2
Methods Six-week randomised, double-blind, two-centre study.
Participants In- and outpatients fulfilling Research Diagnostic Criteria for major depressive disorder, with a score of at least 17 on the HDRS.
Mean age: 46.1 (fluoxetine) and 45.4 (imipramine) years.
Exclusion criteria: significant physical illness, history of drug abuse, schizophrenia, duration of illness more than 1 year
Interventions Fluoxetine: 30 participants.
Imipramine: 30 participants.
Fluoxetine dose range: 40-60 mg/day.
Imipramine dose range: 75-150 mg/day.
Only temazepam was allowed for night sedation.
Outcomes Hamilton Rating Scale for Depression, Montgomery and Asberg Scale for Depression, LPD
Notes Funding: unclear
Risk of bias
Item Authors’ judgement Description
Allocation concealment? Unclear B - Unclear