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Clinical Trials/JPRN-UMIN000001270
JPRN-UMIN000001270
Completed
N/A

The exploratory study about the neurophysiological index which predicts the effect of the methylphenidate hydrochloride in children with AD/HD - The exploratory study about the neurophysiological index which predicts the effect of the methylphenidate hydrochloride in children with AD/HD

niversity of Tokyo Medical School The department of Psychiatry0 sites30 target enrollmentAugust 1, 2008

Overview

Phase
N/A
Intervention
Not specified
Conditions
Attention deficit hyperactivity disorder
Sponsor
niversity of Tokyo Medical School The department of Psychiatry
Enrollment
30
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 1, 2008
End Date
June 30, 2011
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of Tokyo Medical School The department of Psychiatry

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\.A child who is judged that he/she cannot obey and understand the instruction of this trial by the investigator. 2\.A child who weighs under 20kg. 3\.A child who is diagnosed now with critical undesirable diseases to this trial. 4\.A child who has abnormalin the examination of 12\-lead electrocardiogram. 5\.A child who has abnormal blood pressure. 6\.A child who is judged by the investigator or subinvestigator of this trial that he/she has inadequate score in clinical examination. 7\.A child who is diagnosed now with glaucoma, thyroidal dysfunction or epilepsia, or has a previous history of those diseases. 8\.A child who is diagnosed now with a motor tic, or the Tourette's syndrome or has a previous or first\-degree family history of Tourette's syndrome. 9\.A child who has a depression that needed a prompt medical treatment of them. 10\.A child who is diagnosed as his/her main disorder with an oppositional defiant disorder, conduct disorder. 11\.A child who is judged that he/she cannot obey and/or understand the instruction of this trial because he/she has both an impaired coordination and a learning disability. 12\.A child who has a full IQ score calculated by WISC\-3 less than 70 points. , 13\.A child who starts a training program after the day of IC acquisition or finishes it before the end of this trial. 14\.The child who has taken the medicine in the dosage exceeding a 60mg/day MPH now. 15\.A child whom hypersensitivity to MPH was shown. Or a child who was judged to have serious side\-effects of MPH. 16\.A child who takes a medicine that combination is prohibited or he/she is judged to need to take it within 7 days before the first day of the behavioral assessment. 17\.The child who has drug abuse, drug intoxication, alcoholism, or first\-degree family history of those diseases 18\.A girl who has her first menstrual period before the start of this trial.

Outcomes

Primary Outcomes

Not specified

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