The multi-center research study will evaluate the safety and effectiveness of PROVIGIL as a treatment for sleep apnea patients who are regular users of CPAP and continue to suffer from daytime sleepiness. PROVIGIL is a medication, which is currently prescribed to treat daytime sleepiness in patients with narcolelpsy (an extreme tendency to fall asleep in quiet surroundings or when engaged in monotonous activities). The purpose of the twelve-week open label extension is to continue safety monitoring.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000040-40
Application #
6414622
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
1974-10-01
Project End
2002-11-30
Budget Start
Budget End
Support Year
40
Fiscal Year
2000
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
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