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| Methods | multicentre, double blind, randomized, placebo controlled, parallel groups | |
| Participants | Senile cerebral insufficiency mild to moderate; 82 patients received nicergoline, 80 placebo; age > 55 yr. | |
| Interventions | Nicergoline or Placebo 20mg. twice a day (os) for 6 months | |
| Outcomes | SCAG for efficacy; adverse events for safety | |
| Notes | It describes also a crossover study but with no data available for inclusion in this review | |
