Using Methylphenidate to Treat Adults with ADHD
Official title: Methylphenidate in Adults With Attention Deficit/Hyperactivity Disorder
Run by Hospital de Clinicas de Porto Alegre · NCT02951754 · Data updated 2026-11-12
This study is testing how well a common ADHD medication called Methylphenidate works for adults and if certain factors can help predict who will benefit from it.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 600 (estimated) |
| Sponsor | Hospital de Clinicas de Porto Alegre Academic / other |
| Locations | 1 site (Porto Alegre, Rio Grande do Sul) |
| Status | Recruiting |
| Started | February 2002 |
| Main results expected | December 2032 |
| Study ends | December 2032 |
| Registry record updated | November 1, 2016 |
| Trial ID | NCT02951754 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are White Brazilian adults of European descent diagnosed with ADHD who are eligible for immediate-release Methylphenidate treatment.
✕Probably not a fit
Patients with contraindications for Methylphenidate, current stimulant treatment, or significant neurological diseases may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates the effectiveness of Methylphenidate (MPH), a common treatment for adults with Attention-Deficit/Hyperactivity Disorder (ADHD). It aims to identify clinical and genetic factors that predict how well patients respond to MPH, given the variability in treatment outcomes. Participants will receive immediate-release MPH while researchers will monitor their responses and tolerability. The study seeks to enhance understanding of personalized treatment approaches for ADHD in adults.
Why it matters
Potential benefit: If successful, this study could lead to more tailored and effective treatment strategies for adults with ADHD.
How similar studies have gone: Previous studies have shown that Methylphenidate is effective for ADHD, but this study's focus on genetic predictors is a novel approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
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
Where it's running
-
Program on Attention-Deficit/Hyperactivity Disorder (PRODAH); Hospital de Clínicas de Porto Alegre
Porto Alegre, Rio Grande do Sul, Brazil Recruiting
Study contacts
- Principal investigator: Eugênio H Grevet, MD, PhD — Hospital de Clinicas de Porto Alegre
- Study coordinator: Eugênio H Grevet, MD, PhD
- Email: ehgrevet@gmail.com
- Phone: +55 51 3359-8094
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.