To investigate the effects of Souvenaid in elderly patients at high risk of developing Alzheimer’s disease.
The primary outcome measure is cognitive performance assessed by a modified version of the Neuropsychological Test Battery (NTB)
The EU-funded LipiDiDiet™ study is a 24-month, randomised, controlled, double-blind, parallel-group, study aiming to recruit 300 prodromal Alzheimer’s disease subjects. Patients will be randomised to receive Souvenaid or an isocaloric control drink. Enrolment for the study is now complete, with first results expected at the end of 2015.
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