Phase
Condition
N/ATreatment
N/AClinical Study ID
Ages 18-40 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
18-40 years of age
Able to give informed consent for study participation
Sufficient fluency in English to understand and complete the neuropsychological tasks
Exclusion
Exclusion Criteria:
Current usage of other regular medication (including the contraceptive pill, theDepo-Provera injection or the progesterone implant, and hormone replacement therapy)
Any past or current Axis 1 DSM-IV psychiatric disorder
Significant medical condition
Pulse < 60 beats per minute at baseline screening
Current or past gastro-intestinal disorder or irritable bowel syndrome
Current pregnancy or breastfeeding
Known lactate deficiency or any other problem absorbing lactose, galactose or glucose
Current or past history of drug or alcohol dependency
Participation in a psychological or medical study involving the use of medicationwithin the last 3 months
Previous participation in a study using the same, or similar, emotional processingtasks
Smoker > 5 cigarettes per day
Typically drinks > 6 caffeinated drinks per day
Study Design
Study Description
Connect with a study center
University of Oxford
Oxford, Oxfordshire OX3 7JZ
United KingdomActive - Recruiting

Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.