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RECRUITING
NCT02951754
PHASE4

Methylphenidate in Adults With Attention Deficit/Hyperactivity Disorder

Sponsor: Hospital de Clinicas de Porto Alegre

View on ClinicalTrials.gov

Summary

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.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

600

Start Date

2002-02

Completion Date

2032-12

Last Updated

2016-11-01

Healthy Volunteers

No

Interventions

DRUG

Immediate-release Methylphenidate

Standard initial dose of 10 mg, twice or three times daily with doses increasing weekly until symptom control or occurrence of limiting adverse effects

Locations (1)

Program on Attention-Deficit/Hyperactivity Disorder (PRODAH); Hospital de Clínicas de Porto Alegre

Porto Alegre, Rio Grande do Sul, Brazil