Study | Study Design | Follow-up | Risperidone n/N (%) | Placebo n/N (%) | RD | NNT | |
---|---|---|---|---|---|---|---|
Clinical End Point | |||||||
>50% Improvement in Behave-AD 1 total score | |||||||
 | Katz [62] | Double-blind placebo controlled RCT (n=625) | 12 weeks | (45%) | (33%) | 12% | 8 |
 | Schneider [6] | Meta Analysis of 3 studies (n=1001) | 12 weeks | 266/574 (46%) | 139/427 (33%) | 14% | 7.4 |
>30% Improvement in Behave-AD 1 total score | |||||||
 | DeDeyn [8] | Double-blind placebo controlled RCT (n=344) | 12 weeks | (72%) | (61%) | 11% | 9 |
CGI-C 2 (much/very much improved) | |||||||
 | Brodaty [61] | Double-blind placebo controlled RCT (n=93) | 12 weeks | 27/46 (59%) | 12/47 (26%) | 33% | 3.3 |
 | Schneider [6] | Meta Analysis of 2 studies (n=717) | 8-12 weeks | 227/351 (65%) | 175/366 (48%) | 17% | 6 |
 | Katz [5] | Meta Analysis of 4 studies (n=889) | End point | (28%) | (17%) | 11% | 9 |
 | Sultzer [63] | Double-blind placebo controlled RCT (n=421) | 12 weeks | (61%) | (40%) | 21% | 5 |