Attention-Deficit Hyperactivity Disorder (ADHD) in Adults
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adults, ADHD diagnosis, normal hearing, normal or corrected to normal vision Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) F.1.3.1 Number of subjects for this age range
Exclusion criteria
Exclusion criteria: Current history of neurological and/or psychiatric disorders, history of movement disorders, epilepsy, current use of MAO inhibitors or coumarin anticoagulants, drug abuse, problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption, severe hypertension, cardiac arrhythmia, angina pectoris, hyperthyroidism, glaucoma, thyrotoxicosis, pregnancy, severe hand motor deficit
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: To provide an objective tool for the diagnosis and treatment monitoring of ADHD.;Secondary Objective: To improve the diagnosis and treatment of ADHD in adulthood, and throught it, the quality of life of these patients and their families.;Primary end point(s): Normalisation of event-related brain potentials (ERPs), improved behavioural measures | — |
Countries
United Kingdom