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| Methods | Six‐week, randomised study |
| Participants | Patients with depression according to CCMD‐III criteria |
| Interventions | Citalopram: 26 participants Fluoxetine: 25 participants Citalopram dose‐range: 20‐60 mg/day Fluoxetine dose‐range: 20‐60 mg/day |
| Outcomes | Hamilton Depression Rating Scale 17‐Item (HDRS‐17) |
| Notes | Waiting for translation from Chinese to English (only abstract available in English) |
