Clinical Trials Directory

Trials / Terminated

TerminatedNCT01017263

Vyvanse and Glucose Intolerance in Children With Attention Deficit Hyperactivity Disorder (ADHD) and Obesity

Vyvanse and Glucose Intolerance in Children With ADHD and Obesity

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
14 (actual)
Sponsor
Duke University · Academic / Other
Sex
All
Age
8 Years – 17 Years
Healthy volunteers
Accepted

Summary

The purpose of this study to assess the effects of chronic administration of Vyvanse (lis-dexamphetamine) on glucose metabolism in a sample of children and adolescents with Attention Deficit Hyperactivity Disorder (ADHD) who also have glucose intolerance and are obese.

Conditions

Interventions

TypeNameDescription
DRUGLis-dexamphetamineEligible subjects will be dispensed open label LDX (VyvanseTM). All subjects will start at 20 mg once a day dose and will be titrated up weekly by 10 mg increments up to a maximum dose of 70 mg. If a subject experiences intolerable side effects at a particular dose, a step down to the next tolerated level is allowed.

Timeline

Start date
2009-12-01
Primary completion
2012-08-01
Completion
2012-08-01
First posted
2009-11-20
Last updated
2014-02-20
Results posted
2014-02-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01017263. Inclusion in this directory is not an endorsement.