findmyKOL
Clinical trialNCT02797678CompletedInterventional

Feasibility, Effectiveness and Efficacy of the PowerSleep Device

SponsorPhilips RespironicsEnrollment62SleepSleep Disorders Not Due to A Substance or Known Physiological Condition
View the registry record on ClinicalTrials.gov

Summary

The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

4 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Neurotrials Research Inc

    Atlanta, Georgia, United States

  • St. Lukes Hospital

    Chesterfield, Missouri, United States

  • Clayton Sleep Institute

    St Louis, Missouri, United States

  • University of Pennsylvania

    Philadelphia, Pennsylvania, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
30 Jun 2016
Primary completion
31 Dec 2016
Completion
31 Jan 2017
Last update posted
11 Jan 2019
Registered enrollment
62
Registry id
NCT02797678

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.