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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 study.
Participants Outpatients fulfilling DSM-III criteria for current major depressive disorder, with a score between 18 and 25 on the HDRS-21.
Age range: 18-65 years old.
Exclusion criteria: organic brain disease, history of seizures, serious illness, including cardiovascular, hepatic, renal, respiratory, hematologic, hyperthyroidism, history of severe allergy or multiple drug reaction, history (less than 1 year) of drug and alcolhol abuse, concurrent administration of psychotropic drugs (a part from benzodiazepines), MAOI within 2 weeks, serious suicidal risk, pregnancy, lactation
Interventions Fluoxetine: 71 participants.
Clomipramine: 72 participants.
Fluoxetine dose: 20 mg/day.
Clomipramine dose: 75 mg/day.
Outcomes Hamilton Rating Scale for Depression (HDRS-21)
Notes Funding: unclear
Risk of bias
Item Authors’ judgement Description
Allocation concealment? Unclear B - Unclear