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Methylphenidate in Adults With Attention Deficit/Hyperactivity Disorder

RecruitingPhase 4Ages 18 Years - anyAllHospital de Clinicas de Porto Alegre
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In plain words

What the trial is, and whether it could suit you

Methylphenidate (MPH) is the first-line pharmacological treatment for adults with Attention-Deficit/Hyperactivity Disorder (ADHD). Nevertheless, there is considerable interindividual variability regarding the dose required, tolerability and response rates to MPH. The aim of this study is to address the clinical and genetic predictors of MPH treatment outcomes in ADHD.

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: * White Brazilian of European descent * Fulfillment of the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, (DSM-IV) diagnostic criteria for ADHD * Eligibility to immediate-release MPH (IR-MPH) treatment Exclusion Criteria: * Contraindication for IR-MPH use * Current stimulant treatment * Evidence of a clinically significant neurological disease that might affect cognition (e.g., delirium, dementia, epilepsy, head trauma, and multiple sclerosis) * Current or past history of psychosis * Estimated intelligence quotient score lower than 70
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What it tests

  • Immediate-release Methylphenidate
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Where

1 site
Program on Attention-Deficit/Hyperactivity Disorder (PRODAH); Hospital de Clínicas de Porto Alegre
Porto Alegre, Brazil
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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