Huang b 2006.
Methods | Eight‐week, (likely) randomised study. |
Participants | Out‐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 | Change in Hamilton Depression Rating Scale (HDRS) from baseline to endpoint, number of patients who responded to treatment. |
Notes | Waiting for translation from Chinese to English (only abstract available in English). |