Geen aandoening, dit onderzoek richt zich op de werking van het gezonde brein. Not applicable
Conditions
Interventions
Participants will receive 40mg atomoxetine, 5mg donepezil, 20mg memantine or
placebo on four different test sessions, in a randomized order.
Sponsors
Universiteit van Amsterdam
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Healthy volunteers between 18 and 30 years old; Native Dutch speakers; Predominant right-handedness; BMI between 18.5 and 30. Male
Exclusion criteria
Exclusion criteria: Current or history of any medical or psychiatric disorder or disease Smoking Allergy for atomoxetine, donepezil, memantine or one of the inactive ingredients of these products
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary study parameters include behavioral reaction times and performance scores and EEG-, MEG- and fMRI-measures. | — |
Countries
Netherlands
Outcome results
None listed