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| Methods | multicentre, double blind, randomized, placebo controlled, parallel groups | |
| Participants | SDAT mild to moderate; 74 patients received nicergoline, 75 placebo; age > 50 yr. | |
| Interventions | Nicergoline or Placebo 30mg. twice a day (os) for 6 months | |
| Outcomes | ADAScog, CGIC for efficacy; adverse events for safety | |
| Notes | ITT (LOCF) analysis is available | |
