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
| Type | Name | Description |
|---|---|---|
| DRUG | Lis-dexamphetamine | Eligible 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.