Pan 2005.
Methods | Eight‐week, (likely) randomised study. |
Participants | In‐patients with depression according to CCMD‐ III criteria. |
Interventions | Citalopram: 30 participants. Paroxetine: 30 participants. Venlafaxine: 30 participants. Citalopram dose range: 20‐60 mg/day. Paroxetine dose range: 20‐50 mg/day. Venlafaxine dose range: 75‐375 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). |