DEC-NET Serial number GB275 |
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Published online | 07/07/2004 11.51.00 |
Last updated | 02/08/2005 12.33.24 |
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Other protocol ID number | N0544122074 |
This trial has been approved by an ethics committee |
Current trial status | Open (actively recruiting new participants) |
First subject enrolment Target N. of subjects |
01/2003 30 |
Major Disease (ICD9 class) | ATTENTION DEFICIT DISORDER OF CHILDHOOD |
Experimental drug |
Methylphenidate
Treatment regimen (dosage and duration) N/A |
Gender | Male |
Age (range) | 7-13 years |
Eligibility criteria |
Inclusion criteria |
Diagnosed with Attention deficit disorder. |
Exclusion criteria |
Previously had Methylphenidate
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Trial design/methodology |
Phase | 3 |
Kind of study | Efficacy Safety
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Design | Controlled Randomised Blinded Double blind
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Purpose of study |
To investigate effects of Methylphenidate on decision-making, response inhibition and delay processing in seven to thirteen year old boys diagnosed with ADHD. Furthermore, the project will examine relationships between the identified cognitive abnormalities and clinical/ behavioural symptoms. |
Primary outcomes |
Effects of Methylphenidate on decision-making, response inhibition and delay processing. |
Secondary outcomes |
To clarify the nature of, and the relationships between, neurochemical, cognitive and behavioural phenotypes of this disorder. |
Summary of study design, objectives, and ongoing research findings |
Double-blind, placebo-controlled study to investigate the effects of Methylphenidate on decision-making, response inhibition and delay processing in seven to thirteen year old boys with ADHD. The project also aims to clarify the nature of, and the relationships between, neurochemical, cognitive and behavioural phenotypes of this disorder.
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