Effects of tramadol on cognitive functions in normal subjects using fMRI
Not Applicable
Recruiting
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000015889
- Lead Sponsor
- ippon Medical School
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 35
Inclusion Criteria
Not provided
Exclusion Criteria
Subjects with drug allergy. Subjects with history of epilepsy or seizure. Subjects taking drugs within 2 weeks of the trial. Subjects with liver or renal dysfunction. Subjects who have tendency to drug abuse or drug dependence. Pregnant woman and woman suspected of being pregnant. Woman who is breastfeeding. Subjects with contraindications to MRI. Subjects who are judged as not suitable for participation in this study.
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 tramadol conditions
- Secondary Outcome Measures
Name Time Method