Trials / Terminated
TerminatedNCT00626210
Modafinil Treatment for Sleep/Wake Disturbances in Older Adults
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 2 (actual)
- Sponsor
- VA Palo Alto Health Care System · Federal
- Sex
- All
- Age
- 50 Years
- Healthy volunteers
- Not accepted
Summary
Modafinil, trade named Provigil, is a medication approved by the Food and Drug Administration for the treatment of narcolepsy, obstructive sleep apnea/hypopnea syndrome, and shift work sleep disorder. Each of these problems is characterized by difficulty sleeping at night and excessive daytime sleepiness. Modafinil is prescribed during the day to counteract this sleepiness. The idea behind this treatment is that sleepiness that leads to napping during the day prevents a patient from being tired or sleepy enough to get good sleep at night. This study is designed to determine if the medication can "reset" participants' sleep/wake rhythm to a more normal rhythm.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | modafinil | 100-400 mg daily for 4 weeks |
Timeline
- Start date
- 2008-02-01
- Primary completion
- 2011-04-01
- Completion
- 2012-10-01
- First posted
- 2008-02-29
- Last updated
- 2019-10-28
- Results posted
- 2014-10-30
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00626210. Inclusion in this directory is not an endorsement.