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
| Type | Name | Description |
|---|---|---|
| GENETIC | norepinephrine 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.