None
Conditions
Interventions
Experimental group:Phase I: Orally taking acetaminophen
Sponsors
Beijing Normal University
Eligibility
Sex/Gender
All
Age
18 Years to 30 Years
Inclusion criteria
Inclusion criteria: 1. Healthy humanity aged 18-30 years; 2. Dextromanuality.
Exclusion criteria
Exclusion criteria: 1. Take the medicine for illness or other reasons within 1-2 weeks before the experiment; 2. Currently suffering from physical diseases; 3. Smoking more than 10 cigarettes a day, drinking more than 5 liters per day (such as beer); 4. Suffering from claustrophobia; 5. Those who are allergic to aspirin or acetaminophen; 6. Liver and kidney dysfunction; 7. Pregnant women and lactating women; 8. With mental illness, neurological disease, taking acetaminophen-containing drugs or interacting with acetaminophen; 9. With metal in the body: dentures (filling teeth or ceramic teeth), braces, etc.; electronic implant devices such as pacemakers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Moral preference; | — |
Countries
China
Contacts
Public ContactYina Ma
State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University
Outcome results
None listed