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

H

Hallym University

Status and phase

Completed
Phase 4

Conditions

Methylphenidate
Attention Deficit Disorder With Hyperactivity
Pharmacogenetics

Treatments

Genetic: norepinephrine transporter polymorphism,

Study type

Interventional

Funder types

Other

Identifiers

NCT00757029
NETADHD

Details and patient eligibility

About

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.

Enrollment

150 estimated patients

Sex

All

Ages

6 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ADHD
  • Physically healthy

Exclusion criteria

  • Neurological illness
  • Concurrent additional psychiatric treatment
  • < IQ 70
  • Psychotic disorder
  • Major mood disorder needed other psychiatric medication
  • Significant suicidal ideation
  • Pervasive developmental disorder

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

150 participants in 1 patient group

open label
Other group
Treatment:
Genetic: norepinephrine transporter polymorphism,

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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