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eurocognitive testing in children with ADHD

Conditions
Attention Deficit Hyperactivity Disorder
MedDRA version: 9.1Level: LLTClassification code 10003735Term: Attention deficit-hyperactivity disorder
Registration Number
EUCTR2008-004425-42-NL
Lead Sponsor
Centre for Human Drug Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

•Written informed consent from parents having parental responsibility or from the legal guardian. In the case of a child aged 12 years the written informed consent of the child is needed in addition to that of parents having responsibility/legal guardian;
•Aged 8-12 years;
•Able to communicate with the investigator in Dutch;
•Confirmed DSM IV diagnosis of ADHD (Based on examination by a psychiatrist or pediatrician);
•Classifying as clinical ADHD on the AVL(ADHD Vragenlijst”);
•Currently receiving treatment with (immediate or sustained release) methylphenidate

Are the trial subjects under 18? yes
Number of subjects for this age range:
F.1.2 Adults (18-64 years) no
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

•Use of drugs other than methylphenidate with known psychotropic effects.

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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