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NCT01175031 · ClinicalTrials.gov registry record · NA
Comparison of Breathing Event Detection by a Continuous Positive Airway Pressure Device to Clinical Polysomnography
A NA study of Obstructive Sleep Apnea and Cheyne-Stokes Respiration, sponsored by Philips Respironics.
- Completed
- Registry status
- NA
- Development phase
- 45
- Enrollment target
- 3
- Study locations
NCT01175031 is a NA study of Obstructive Sleep Apnea and Cheyne-Stokes Respiration that has completed, run by Philips Respironics. The registered enrollment target is 45 participants, below the 221-participant average among 155 other Obstructive Sleep Apnea trials with a reported enrollment target (80% lower). The trial reports 3 study locations across 3 states.
The verdict
NCT01175031, a NA study of Obstructive Sleep Apnea and Cheyne-Stokes Respiration, has completed, sponsored by Philips Respironics.
- COMPLETED
- Registry status
- NA
- Development phase
- 45 participants
- Enrollment target
- 3
- Study locations
Study Summary
The purpose of this study is to demonstrate diagnostic agreement and determine the accuracy of the continuous positive airway pressure (CPAP) device compared to simultaneous, attended clinical polysomnography (PSG) in identifying breathing events in participants previously diagnosed with complex sleep apnea (CompSAS), complex sleep apnea with Cheyne-Stokes respiration (CSR), or obstructive sleep apnea (OSA).
Conditions Studied
Interventions
- OTHER Manipulation of Positive Airway Pressure (PAP)
Study Locations (3)
Colorado
- National Jewish Health - Denver
Florida
- University of Florida - Shands Sleep Disorders Center - Gainesville
Michigan
- Sleep Health - Portage
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 45 participants |
| Start Date | 2010-09 |
| Est. Completion | 2013-09 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01175031
The ClinicalTrials.gov registry entry for NCT01175031 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 221-participant average among 155 other Obstructive Sleep Apnea trials with a reported enrollment target (80% lower). The listed sponsor is Philips Respironics, which has 35 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Obstructive Sleep Apnea appearing as the primary indexed condition, and to 1 intervention - of which Manipulation of Positive Airway Pressure (PAP) is the first listed.
NCT01175031 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Colorado, Florida, Michigan.
Frequently Asked Questions
What is clinical trial NCT01175031 about?
NCT01175031 is a clinical study titled "Comparison of Breathing Event Detection by a Continuous Positive Airway Pressure Device to Clinical Polysomnography". The purpose of this study is to demonstrate diagnostic agreement and determine the accuracy of the continuous positive airway pressure (CPAP) device compared to simultaneous, attended clinical polysomnography (PSG) in identifying breathing events in participants previously diagnosed with complex sle...
What is the current status of trial NCT01175031?
This trial is currently completed. It is a NA study. The enrollment target is 45 participants. The study started on 2010-09. Estimated completion is 2013-09.
What conditions does trial NCT01175031 study?
This clinical trial studies the following conditions: Obstructive Sleep Apnea, Cheyne-Stokes Respiration, Sleep Apnea Central.
What interventions are being tested in trial NCT01175031?
The interventions under investigation include: Manipulation of Positive Airway Pressure (PAP) (OTHER).
Who is sponsoring clinical trial NCT01175031?
This trial is sponsored by Philips Respironics, which has 35 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01175031 being conducted?
This trial has 3 study locations across Colorado, Florida, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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