Skip to main content
. 2008 Jan 23;2008(1):CD001765. doi: 10.1002/14651858.CD001765.pub3

Goodman 1989.

Methods Design: RCT parallel group, Blindness: double (but in fact triple) Duration of study: 6 wks
Participants Single or multicentre: Multicentre Diagnostic criteria: DSM III Co‐morbidity allowed: Secondary depression including sever Setting: Outpatients Age: Mean (SD) 39(14) to 35(11) Other characteristics: Men and women
Interventions No. of arms: Two ‐ Fluvoxamine versus placebo
Outcomes Primary: 
 Change in YBOCS total score
Proportion of responders (defined as CGI of 1 or 2)
Notes 3
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear