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Effects of modafinil on cognitive functions in normal subjects using fMRI

Not Applicable
Conditions
healthy adults
Registration Number
JPRN-UMIN000007324
Lead Sponsor
ippon Medical School
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
25
Inclusion Criteria

Not provided

Exclusion Criteria

Subject with arrhythmia and drug allergy. Subject with history of heart diseases and epilepsy. Subjust taking drugs within 2 weeks of the trial. Subject with contraindications to MRI.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Comparison of BOLD signal changes measured by fMRI between placebo and modafinil conditions.
Secondary Outcome Measures
NameTimeMethod
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