drugset / Trial / NCT02635035
Shire SCT: Lisdexamfetamine Treatment for ADHD and SCT
RandomizedCrossoverDouble-blindTreatment
Summary
The primary purpose of this study is to test the efficacy of Lisdexamfetamine in Adults With Attention Deficit Hyperactivity Disorder (ADHD) and Sluggish Cognitive Tempo (SCT). This is a placebo controlled, cross-over clinical trial of oral Lisdexamfetamine Dimesylate 30-70mg/day in adults with attention-deficit hyper-activity disorder and Sluggish Cognitive Tempo (ACT). Patients will be assigned either LDX/Placebo for 10 weeks with a two week placebo washout period.
Timeline
- Start
- 2015-11
- Primary completion
- 2019-01-09
- Completion
- 2019-01-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Lisdexamfetamine | Other / unclassified | 30 mg | Oral |
| Subject | Lisdexamfetamine | Other / unclassified | 50 mg | Oral |
| Subject | Lisdexamfetamine | Other / unclassified | 70 mg | Oral |