Zhao 2006.

Methods	Eight‐week, (likely) randomised study.
Participants	In‐ and out‐patients with depression according to CCMD‐III criteria.
Interventions	Citalopram: 30 participants. Fluoxetine: 30 participants. Citalopram dose range: 20‐60 mg/day. Fluoxetine dose range: 20‐60 mg/day.
Outcomes	Change in Hamilton Depression Rating Scale 24 Item (HDRS‐24) score from baseline to endpoint, number of patients who responded to treatment.
Notes	Waiting for translation from Chinese to English (only abstract available in English).