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| Methods | Four‐week, randomised study |
| Participants | Patients with depression according to CCMD‐III criteria |
| Interventions | Sixty patients randomised to fluoxetine or reboxetine Fluoxetine dose range: 4‐8 mg Reboxetine dose range: 20‐40 mg |
| Outcomes | Hamilton Depression Rating Scale (HDRS) and Clinical Global Impression (CGI) |
| Notes | Waiting for translation from Chinese to English (only abstract available in English) |
