Methylphenidate vs. Risperidone for the Treatment of Children and Adolescents With ADHD and Disruptive Disorders
Attention Deficit/Hyperactivity Disorder, Oppositional Defiant Disorder, Conduct Disorder
About this trial
This is an interventional treatment trial for Attention Deficit/Hyperactivity Disorder focused on measuring ADHA, ODD, Conduct disorder, Aggression, Treatment, Methylphenidate, Risperidone
Eligibility Criteria
Inclusion Criteria:
- Clinical diagnosis of ADHD (any sub-type) with oppositional defiant disorder.
- Clinical diagnosis of ADHD (any sub-type) with conduct disorder.
- Clinical diagnosis of other specified ADHD with oppositional defiant disorder.
- Clinical diagnosis of other specified ADHD with conduct disorder.
- Clinical diagnosis of unspecified ADHD with oppositional defiant disorder.
- Clinical diagnosis of unspecified ADHD with conduct disorder.
Exclusion Criteria:
- Participant who do not qualify for inclusion criteria.
- Participant who are not willing to join the study.
- Epilepsy.
- Neuro-genetic syndromes.
- Brain tumors.
- Autism.
- Participants who are under psychiatric medication and have changed it (dose or kind) in the last month.
- Congenital heart, kidney of liver defects.
- Cardiomyopathies.
- Past hypersensitivity to Methylphenidate or Risperidone.
Sites / Locations
- Sheba medical center
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Methylphenidate
Risperidone
Participants in this arm will be given either "Concerta" - a long acting (12 hours) Methylphenidate pill - once daily, in the morning (starting dose 1 mg/kg, max dose 2 mg/kg), or "Ritalin LA" - a long acting (10 hours) Methylphenidate pill - once daily, in the morning (starting dose 0.6 mg/kg, max dose 1.5 mg/kg) for children who can not swallow pills.
Participants in this arm will be given a low dose of Risperidone. Starting dose will be 0.5 mg/d, max dose will be 2 mg/d.