Effects of bupropion on cognitive functions in normal subjects using fMRI
Not Applicable
Recruiting
- Conditions
- healthy adults
- Registration Number
- JPRN-UMIN000007323
- Lead Sponsor
- ippon Medical School
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 25
Inclusion Criteria
Not provided
Exclusion Criteria
Subject with history of seizure disorders and head injury. Subject with contraindications to MRI. Subjust with drug allergy, taking drugs within 2 weeks of the trial and drinking a lot of alcohol. Woman who is breastfeeding. Pregnant woman and woman suspected of being pregnant.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of BOLD signal changes measured by fMRI between placebo and bupropion conditions.
- Secondary Outcome Measures
Name Time Method