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| Methods | Six‐week, randomised, double‐blind, double dummy study |
| Participants | Patients with depression according to CCMD‐III criteria |
| Interventions | 48 participants randomised to fluoxetine or bupropion |
| Outcomes | Hamilton Depression rating scale (HDRS), Hamilton Rating Scale for Anxiety (HAM‐A) and Clinical Global Impression (CGI) |
| Notes | Waiting for translation from Chinese to English (only abstract available in English) |
