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Association of the simultaneous administration of Gingko biloba extract and absorption promoting agent with cognitive functio

Not Applicable
Conditions
Healthy adults
Registration Number
JPRN-UMIN000043494
Lead Sponsor
Department of Aging Research and Geriatric Medicine IDAC, Tohoku University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
155
Inclusion Criteria

Not provided

Exclusion Criteria

1) With past history of severe neurological diseases. 2) With critical bleeding incidents. 3) Use of antithrombotic medicine. 4) Severe depression 5) Patients with diabetes mellitus. 6) With severe visual or auditory disability. 7) Individuals with any metal implantation, such as cardiac pacemaker, coronary stent and artificial joint. 8) Claustrophobia. 9) Use of any supplement. 10) Creatinine clearance less than 15ml/min. 11) Patients with gastrointestinal diseases or metabolic diseases. 12) Diagnosed psychiatric disorders. 13) Participants who cannot obtain the informed consent. 14) Allergy to the study materials. 15) Individuals who is not suitable for participating in this study decided by principal investigator.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary endpoint of this study is to discover any alteration of cognitive function in healthy adults assessed by Wechsler Memory Scale revised (WMS-R) following 24 weeks administration of GBE/MST.
Secondary Outcome Measures
NameTimeMethod
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