NCT02797678View on ClinicalTrials.gov

Feasibility, Effectiveness and Efficacy of the PowerSleep Device

NACompletedINTERVENTIONAL
Enrollment

62

Participants

Timeline

Start Date

June 30, 2016

Primary Completion Date

December 31, 2016

Study Completion Date

January 31, 2017

Conditions
SleepSleep Disorders Not Due to A Substance or Known Physiological Condition
Interventions
DEVICE

Powersleep

Participants will receive 5 nights of stimulation

DEVICE

Sham Powersleep

Participants will receive 5 nights of no stimulation

Trial Locations (4)

19104

University of Pennsylvania, Philadelphia

30342

NeuroTrials Research Inc, Atlanta

63017

St. Lukes Hospital, Chesterfield

63143

Clayton Sleep Institute, St Louis

Sponsors
All Listed Sponsors
lead

Philips Respironics

INDUSTRY

NCT02797678 - Feasibility, Effectiveness and Efficacy of the PowerSleep Device | Biotech Hunter | Biotech Hunter