Clinical trial Recruiting at 1 site Phase 4 Interventional Ages 18 and up

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

PhasePhase 4
Study typeInterventional
Ages18 Years and up
SexAll
Enrollment600 (estimated)
SponsorHospital de Clinicas de Porto Alegre
Academic / other
Locations1 site (Porto Alegre, Rio Grande do Sul)
StatusRecruiting
StartedFebruary 2002
Main results expectedDecember 2032
Study endsDecember 2032
Registry record updatedNovember 1, 2016
Trial IDNCT02951754 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.