[No standalone website (unbranded, no questionnaire)] A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)

How to apply

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Study’s contact

Call center

+55 51 3359-8094

Email address

ehgrevet@gmail.com

Condition

Attention Deficit Disorder With Hyperactivity

Treatment type

Interventional

Investigational product

Immediate-release Methylphenidate

Phase

Phase 4

Sponsor

Hospital de Clinicas de Porto Alegre

ClinicalTrials.gov identifier

NCT02951754

Study number

100358

Date first posted

October 31, 2016

Date last update

October 31, 2016

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About the study

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.

Who can take part?

You may be eligible to participate in the study if you meet the following criteria:

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

For a full list of inclusion/exclusion criteria, please visit ClinicalTrials.gov

Study locations

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How to apply

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