Examination of brain function improvement of plasmalogen intake.
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000024751
- Lead Sponsor
- Shiba Palace Clinic
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Not provided
1 A person who possibly shows food allergy symptom. 2 A person who had been treated, hospitalized or operated for stroke, subarachnoid hemorrhage, cerebral infarction, cerebral haemorrhage, brain contusion or head trauma. 3 A person who is alcohol or nicotine addict, or whose dietary habit is extremely irregular. 4 A person with medical history or current illness of hepatic disorder. 5 A person with severe anemia. 6 A person with medical history of epileptic stroke, diabetes, thyroid dysfunction or severe renal dysfunction(hemodialysis, uremia, anuria), or attending the hospital regularly for these disorder. 7 A person who has taken a neuropsychological test at hospital. 8 A person who joins other human clinical study. 9 A person who is routinely taking medicines (e.g. antipsychotic, antianxiety agent, antidepressant, antiparkinson agent, antimanic agent, anticonvulsant, anticoagulant agent) which possibly affects the test results. 10 A person who is routinely taking health foods (supplements effective for antioxidative, blood flow-ameliorating and so on) which possibly affects the test results. 11 A person who is judged inappropriate to join the study by doctor in charge. (Subject who is judged inappropriate during this test is excluded from targets of analysis. In addition, a criterion not in screening criteria is not included in exclusion criteria for screening.) 12 A person who have taken an RBANS test in 3 month before main test schedule.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method