Clinical Trials Directory

Trials / Completed

CompletedNCT00757029

Pharmacogenetic Study of Methylphenidate in Attention Deficit/Hyperactivity Disorder(ADHD)

Association Between Norepinephrine Transporter Polymorphism and Response of Methylphenidate

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
Hallym University Medical Center · Academic / Other
Sex
All
Age
6 Years – 18 Years
Healthy volunteers
Not accepted

Summary

The noradrenergic system plays a known role in attentional systems and suspected causal role in attention deficit/hyperactivity disorder(ADHD).Methylphenidate also has been suspected as a inhibitor of norepinephrine transporter(SLC6A2). The investigators hypothesis is that norepinephrine transporter polymorphism is associated with responses and adverse effects of OROS-methylphenidate in treatment of ADHD.

Conditions

Interventions

TypeNameDescription
GENETICnorepinephrine transporter polymorphism,OROS methylphenidate (Concerta) monopharmacotherapy dose : 18-54mg duration : 8 weeks genotyping : norepinephrine transporter (SLC6A2) polymorphism

Timeline

Start date
2005-10-01
Primary completion
2008-08-01
Completion
2010-08-01
First posted
2008-09-22
Last updated
2011-10-05

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT00757029. Inclusion in this directory is not an endorsement.