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Clinical Trial Summary

To determine the effect of Armodafinil (Nuvigil) on fatigue and sleep in sarcoidosis.


Clinical Trial Description

The study will be divided into two halves. Patients will receive either drug or placebo in the first half. Patients receiving active drug will be started at one dose and it can be increased at the second visit. Those patients randomized to placebo will also have their dose adjusted by the investigating physician. The physicians will be blinded as to whether the patient is receiving drug or placebo. In the second half of the study, patients will receive the opposite treatment.

Patients will have complete detailed questionnaires regarding their fatigue, sleepiness, and overall quality of life.

They will have sleep studies done at the start and after each half of the study to determine the effect of therapy on sleepiness. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00555347
Study type Interventional
Source University of Cincinnati
Contact
Status Completed
Phase Phase 2/Phase 3
Start date October 2007
Completion date August 2011

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