drugset / Trial / NCT00983437
Study to Evaluate the Safety, Tolerability, and Efficacy of Armodafinil as Treatment for Patients With Excessive Sleepiness Associated With Mild or Moderate Closed Traumatic Brain Injury
Non-randomizedSingle-groupOpen-labelTreatment
Summary
The primary objective of this study is to evaluate the safety and tolerability of long-term (12 months) armodafinil treatment in patients with excessive sleepiness associated with mild or moderate closed traumatic brain injury (TBI).
Timeline
- Start
- 2009-08-31
- Primary completion
- 2011-01-31
- Completion
- 2011-01-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Armodafinil | Small molecule | 150 mg | Oral |
| Subject | Armodafinil | Small molecule | 250 mg | Oral |