Li 2006b.
Methods | Six‐week randomised, double‐blind, double dummy trial |
Participants | Patients with depressive disorder |
Interventions | 228 participants randomised to fluoxetine or reboxetine Fluoxetine dose: unclear Reboxetine dose: unclear |
Outcomes | Hamilton Depression Rating Scale (HDRS) and Clinical Global Impression (CGI) |
Notes | Waiting for translation from Chinese to English (only abstract available in English) |