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COMPLETED NA

Comparison of Breathing Event Detection by a Continuous Positive Airway Pressure Device to Clinical Polysomnography

NCT01175031 · View on ClinicalTrials.gov ↗

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).

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

FieldValue
Enrollment Target 45 participants
Start Date 2010-09
Est. Completion 2013-09
Phase NA

Sponsor

Philips Respironics

9 total trials

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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. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Philips Respironics, which has 9 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01175031 reports 3 study locations spanning 3 distinct geographic areas — top geographies include Colorado, Florida, Michigan. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01175031?

The interventions under investigation include: Manipulation of Positive Airway Pressure (PAP) (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01175031?

This trial is sponsored by Philips Respironics, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial